President`s Message
Transcription
President`s Message
Published by the ISPE San Diego Chapter Serving Southern California San Diego to Orange County Editor: Kimberly Syre Email: [email protected] Information: Phone 1.949.387.9046 and Fax 1.949.387.9047 NEWSLETTER • Volume 16, No. 3 • www.ispe.org/sandiego ISPE’s 2007 and 2008 Platinum First Place Award Winner for Excellence and Innovation In this issue President’s Message PAGES 1 & 2 Full Day Risk Based Validation Class Presentation Descriptions and Speaker Bios PAGES 3-7 Save the Date: April 16 Lean Manufacturing and Six Sigma Meeting at Genentech PAGE 8 DPR Construction group at the January Social Bowling Event at East Village Tavern + Bowl in San Diego. Thanks to DPR and other attendees for participating in the Chapter’s food drive. An entire car load of food was donated to Father Joe’s Villages benefitting needy families in San Diego. Spring Golf Tournament at La Costa Announced PAGES 9-10 Welcome New Chapter Members PAGE 11 Oktoberfest Photos/Overview PAGE 12 Energy Optimization Overview & Genentech Tour Photos PAGE 13 January Social Event Photos PAGE 14 Bioprocessing Class Overview and Photos PAGES 15-16 2009 ISPE Event Calendar PAGE 17 President’s Message I by Andy Darragh of Ferguson Pape Baldwin Architects ’d like to thank Marty Becerra who is stepping down after serving on the ISPE San Diego Board of Directors for over ten years and for being our Treasurer for the past six years. Thank you Marty! Taking her place will be Stacy Sutton, the Assistant Director of Infrastructure and Logistics for Althea Technologies. Help me to welcome Stacy. In November we had another fantastic event at the Genentech NIMO campus in Oceanside. Thanks to Genentech for the delicious spread of food and beverages they provided along with guided tours and a beautiful setting for our workshop on energy optimization. Thanks to Mike Barbera of Project Management Advisors and Carl Hixon of Genentech for organizing this successful event. I hope that many of you were able to attend the ISPE Annual Meeting in Boca Raton, Florida in October, where the San Diego Chapter received the Platinum First Place award for the second year in a row! Thanks to all of you who volunteer your time and attend our events to make our Chapter so strong. We are really looking forward to hosting the Annual Meeting in San Diego this year in November. It’s a rare opportunity for our Members to benefit from the fantastic programs this meeting has to offer without the cost of hotel and airfare. And you can leave your umbrella at home! (continued on next page) President’s Message (continued) This year has already started out strong with a great turnout at our January 15 Social Event at the East Village Tavern and Bowl. We had over 60 attendees for some great bowling, food and fun. We also made a generous donation of canned food for the needy. A special thanks to Ashlee Ujifusa, Christy Pavano and the Membership Committee for all their efforts in putting this event together. Sponsorships Available ISPE Continuing on our theme of Efficiency: Doing More with Less, our January 27 event at Biogen Idec included discussion of the latest in SDG&E rebate programs, air handler and central plant optimization and conversion of cooling towers to use recycled water. With water reduction regulations coming to San Diego soon, this workshop offered some great first-hand knowledge from an owner’s perspective. Classroom Training Lower Production Costs, Improve Process Efficiency, Increase Production Quality, and Meet Regulatory Requirements In February Biogen Idec hosted another great event. Our next newsletter will include event photos and an overview of the meeting. Philadelphia Classroom Training 5-8 October 2009 Hilton Philadelphia Airport, Philadelphia, Pennsylvania, USA In March we are offering our full day education course on RiskBased Validation. This course will consider all facility systems and provide guidance to creating a validation program that addresses risk appropriately without unnecessary overkill. This will be a great overall reference for those involved in systems design and validation. Read on for more details. 09 www.ISPE.org/philadelphiatraining As always, we encourage you to attend events and stay involved. We look forward to seeing you all soon. Andy Products, knowledge, and quality Valin delivers Validation Equipment Calibrations two to three-day typical turnaround Valin is the West’s leading supplier of fluid handling, measurement, process heating, filtration, motion control and automation products for a wide range of bio-pharm and bio-tech applications. Call us today: 1-800-774-5630 Visit us at: www.valin.com or email: [email protected] 1701 E. Edinger Ave. Bldg J. / Santa Ana, CA 92705 Main: 714.953.1635 / Fax: 714.953.2126 Validator 2000 & Digi Strips IRTD, HTR, LTR, CTR RH/CO2 Sensors Hart/Fluke Meters & Probes 2 Validation and Calibration Services 888-433-MASY (6279) www.masy.com Full Day Risk Based Validation Class Wednesday, March 25, 2009 LOCATION: Biogen Idec Nobel Facility 5200 Research Place (UTC Area), San Diego, CA 92122 8:00 am - 5:00 pm Sponsors: Hach Ultra Analytics Inc. R C M Te c h n o l o g i e s , I n c . S i e m e n s B u i l d i n g Te c h n o l o g i e s Program Managers: Dan Cooper Audrey Prosser, QA Manager, Mentor Corporation (J&J) Hosted by: Jerry Yaddgo, Facilities Engineer, Biogen Idec Presenters: Cleaning Validation Presented by AB Allen, Sr. Validation Mgr, Amylin Pharmaceuticals ASTM E2500 and FDA’s Draft Process Validation Guidance: A Comparison and Implementation Presented by Bob Chew, PE, President, Commissioning Agents Inc. Computer Systems Validation Presented by Bob Lucchesi, Global Practice Director, RCM Technologies, Inc. Risk Based Validation, An Auditor’s Perspective Presented by Melissa Hyatt, Sr. QA Auditor, Amylin Pharmaceuticals Current Good Process Validation: Practical Tips and Regulatory Trends Presented by Peter K. Watler, PhD, Principal Consultant & CTO, Hyde Engineering + Consulting, Inc. USP Water System TOC Validation Presented by Paul Farrell, TOC Business Development Manager, Hach Ultra Analytical HVAC Commissioning and Qualification Presented by Jesse Gillikin, cGMP Validation Continental Breakfast and Lunch Provided To Join ISPE On-Line, Visit www.ispe.org 3 Speaker Bios and Class Synopsis For Risk Based Validation Class on March 25th Computer Systems Validation Presented by Bob Lucchesi, Global Practice Director, RCM Technologies, Inc. Presenters: Cleaning Validation Presented by AB Allen, Sr. Validation Mgr, Amylin Pharmaceuticals A high level overview of cleaning validation programs for the pharmaceutical industry will be presented. It will include regulatory requirements and how to establish a cleaning validation program. Anne-Barbara Allen is the Sr. Validation Manager for Amylin Pharmaceuticals. She has been in the pharmaceutical industry for 15 years and prior to that, the aerospace industry for five years. She previously worked for Gensia Sicor, Genentech and most recently Hyde Engineering + Consulting. She received her engineering degree from the U.S. Naval Academy. ASTM E2500 and FDA’s Draft Process Validation Guidance: A Comparison and Implementation Presented by Robert Chew, PE, President, Commissioning Agents Inc. This presentation will review the new FDA draft Process Validation Guidance. This guidance describes validation as being comprised of three major phases over the life of a manufactured drug product or drug substance. The three phases will be discussed. In addition, the specifics surrounding equipment qualification will be highlighted, and contrasted with the provisions of ASTM E2500. Suggestions for improving a qualification program using ASTM E2500 in light of the new FDA guidance will be discussed. Robert Chew is President of Commissioning Agents, Inc., a provider of commissioning, validation, and compliance services. He served on ISPE’s International Board of Directors from 2004 2007. He served on the task team that created ASTM E2500 to improve how the industry does qualification, and is a member of the task team updating ISPE’s Commissioning and Qualification Baseline Guide. He is former chairman of ISPE’s North American Education Committee, ISPE’s International Education Executive Committee, and former President of the ISPE Great Lakes Chapter. He is an official trainer for the ISPE Baseline Commissioning and Qualification Baseline Guide. He has a BS in Chemical Engineering from Case Western Reserve University, and is a registered Professional Engineer. The FDA and the pharmaceutical industry are now recommending guidelines on the validation of computer systems, software, and processes. Learn how to streamline validation costs while optimizing validation procedures. Some topics will include: • Developing a risk based validation program for your company • Categorizing risks and their respective plans • Reducing testing in a risk based environment • Developing a “how to” guide • Developing documentation standards • Differentiating tasks that will reduce time and effort • Impacting strategies for maintenance • Optimizing the Validation Plan Bob Lucchesi is a seasoned professional with over 30 years of experience in various industries and technologies. He is considered a Subject Matter Expert in Life Sciences vertical, especially in validation, quality, content management, and computer systems. The past 19 years have been dedicated almost exclusively to pharmaceutical and medical device consulting. Before this time, he was working in the IT technical arena, beginning with programming and advancing to data base administration and project management. Mr. Lucchesi was also the President of a highly successful consulting firm in the nineties, specializing in program management, process improvement, and infrastructure assessments for the pharmaceutical industry. He is currently the Global Practice Director in the Life Sciences Division of RCM, supporting company staff worldwide in validation, quality, document management, data migration, and overall IT centric needs. (continued on next page) High Purity Liquid Handling Products for Pharmaceutical & Biotech Industries 1-800-726-4835 A Foster Wheeler Company Susanne Lage’ Cost Vice President, Chris Ballew Technical Sales Representative (805) 906-1533 Cell [email protected] 321 Irving Dr., Oxnard, CA 93030 www.sani-techwest.com 4 Business Development • Process Development Emeryville, CA & Scale-Up Direct: 1.510.594.3003 • Critical Utility Design [email protected] • cGMP Upgrades www.biokinc.com • cGMP Facility Design • Debottlenecking • Custom Process Equipment • Commissioning/Qualification/Validation Speaker Bios and Class Synopsis For Risk Based Validation Class on March 25th (continued) Risk Based Validation, An Auditor’s Perspective Presented by Melissa Hyatt, Sr. QA Auditor, Amylin Pharmaceuticals The discussion will address the impact of recent initiatives and the new Draft Guidance on process validation. Examples will be given on how to employ PDA Technical Report 42 concepts, FMEA risk analysis and statistical process control methods to identify and Critical Process Parameters. Stage 3 of the FDA draft guidance will be discussed as well has how to leverage such data to eliminate the burden of formal validation studies and revalidation. Some practical tips on performing mixing studies including what to test, probe placement and family grouping will be provided. The discussion will address how to reduce the burden of membrane and chromatography re-use validation by applying PAT and enhanced statistical monitoring. Implications from These 21st Century approaches support better quality, higher compliance, and at the same time lowering costs. Melissa will provide insight on how an auditor views Risked Based Validation. The presentation will discuss documentation and questions that could typically occur during an auditor’s review of risk based validations associated with new facilities or cleaning. Additionally, it will include a review of current trends of agency observations related to inadequate validation activities. Melissa Hyatt has been working in the pharmaceutical/biotech industry in for more than 10 years. She started her career in the Quality Control Analytical and Microbiology Laboratories of Aventis, then worked as a Validation Consultant at FBN Validation Associates. Since 2003 she has been a Quality Auditor at American Pharmaceutical Partners, based in the great Chicago area and currently at San Diego based Amylin Pharmaceuticals. Melissa is a cGMP Certified Auditor through ISPE/GMP Institute and a Certified Quality Auditor through ASQ. She has audited GXP facilities throughout the US, Europe, Asia, and South America. Current Good Process Validation: Practical Tips and Regulatory Trends Presented by Peter K. Watler, PhD, Principal Consultant & CTO, Hyde Engineering + Consulting, Inc. Peter Watler, PhD is Principal Consultant and Chief Technology Officer with Hyde Engineering + Consulting. He has 21 years of GMP biopharmaceutical process experience with a focus on process design, scale-up, implementation and facility design, start-up and qualification. He has prepared three license submissions and participated in several FDA inspections and GMP audits. Dr. Watler was previously Vice President, Manufacturing at VaxGen, where he led the design, construction, commissioning and qualification of a GMP vaccine facility. He was also responsible for managing supply chain and production operations, led the CMC team and prepared submissions for government agencies. He previously spent 12 years at Amgen, leading process development, manufacturing support and overseeing pilot plant operations. He has led teams for technology transfer, scale-up, pre-clinical production and process validation for Neupogen®, Stemgen®, Kepivance® and Infergen®. Dr Walter holds a Bachelor’s and a Master’s degree in Chemical Engineering from the University of Toronto and a PhD in Chemical Engineering from Yamaguchi University, Japan. The 1990s saw the FDA increase its scrutiny of utility systems, QC laboratories and facility operations. The new millennium has seen a tremendous shift in focus, with regulatory emphasis on process validation. Initiatives such as Quality by Design (QbD), Design Space concepts and Process Analytical Technologies (PAT) are forming the basis of a current Good Process Validation (cGPV). Process validation now extends far beyond testing process streams for yield and purity to include concepts such a Critical Process Parameters, Design of Experiments (DOE), orthogonal analytical methods and justified acceptance criteria. These advances culminated with the FDA issuing draft Guidance for Industry, Process Validation: General Principles and Practices in November 2008. While the FDA has been advocating more scientific practices as outlined in the guidance, this is nonetheless the first formal update in 20 years, and will dramatically alter and align industry practices. VALIDATION (continued on next page) COMMISSIONING Engineering Architecture Process Technology Process Automation Systems Integration Construction Management TRAINING Nino Borsoni, PMP - Senior Vice President [email protected] p. 925.363.3112 f. 925.689.7006 AUDITS 500 Airport Blvd, Suite 100 • Burlingame, CA 94010 Toll-Free (888) 242-0559 • Office (650) 320-1788 • Fax (650) 320-1789 www.propharmagroup.com 5 Startup & Commissioning Procurement Project Management Speaker Bios and Class Synopsis For Risk Based Validation Class on March 25th (continued) USP Water System TOC Validation Presented by Paul Farrell, TOC Business Development Manager, Hach Ultra Analytical the system offers advantages because of the levels of purity found in today’s systems and the lower detection capabilities of on-line analyzers. It is best to use both methods to ensure complete understanding of the water systems capabilities in all situations. Pharmaceutical companies are in the business of manufacturing drugs or ingredients for drugs, and though drug production is the final goal it is not the largest volume item they typically produce. In fact what a great many pharmaceutical facilities produce the most of in bulk quantities is water and more specifically USP water. The USP water system travels throughout the facility and affects all the areas in a facility. USP water is used in manufacturing during the process, in manufacturing after production for cleaning, to make Clean Steam and in some of the laboratory process for making standards and reagents. Validation testing should be conducted under different conditions of the water manufacturing process; these include at rest, during high and low production and depending on the location at different times of the year. Seasonal and environmental changes will effect the feedwater which will test the effectiveness of the pretreatment system to supply quality water. Paul Farrell is the Global TOC Business Development Manager at Hach Ultrapure group. Paul is the lead presenter and coordinator of Hach Ultra’s “Pharmaceutical Water Monitoring” program in Hach Ultra’s Life Science Users Group (LSUG) seminars and speaks at industry conferences. TOC is a required measurement of USP waters. All water systems designed to provide Purified Water, Water For Injection or Clean Steam need to meet TOC levels described in the Chapter <643> of the USP Monographs. Paul began work in the pharmaceutical business in 1980 with Kaye Instruments and has been in the Ultrapure water business for 17 years. He was National Sales manager for Thornton from 1992-98. Paul helped to promote the establishment of the USP 23 changes to conductivity by presenting papers on this subject at the 1996 National Conference of Standards Laboratories (NCSL) and various ISPE Conferences. Validation of the USP water systems ability to meet the TOC specification requires validated and qualified equipment. Testing is done to ensure performance specified in the water system User Requirement Specification is met. As part of the validation document it should clearly define the locations in the system where sampling will be done. HVAC Commissioning and Qualification Presented by Jesse Gillikin, cGMP Validation The TOC validation testing is accomplished using a combination of on-line and laboratory sampling. Although it is quite common to see only lab sampling as part of the validation testing, including on-line for the high purity and USP parts of The session will provide practical approaches to commissioning and qualification with emphasis on risk-based approach as described in the ISPE Guidelines, GAMP5, and ASTM E-2500. Practical boundaries for commissioning and qualification of the AHUs (air handler units), BMS (Building Management System), and Facility Qualifications will be discussed. No Standard Is Too High For ABC. Jesse is a co-founder of cGMP Validation and serves as the President and CEO. Jesse has over 30 years of experience in the pharmaceutical industry, including working with more than 300 companies regarding validation and compliance practices. ALLEGHENY BRADFORD CORPORATION Regional Manager - Dori Carlson Skids • Tanks • Valves • Pumps Heat Exchangers • Filter Housings 1522 South Ave., Lewis Run, PA 16738 800-542-0650 • www.alleghenybradford.com Validation Equipment Rentals Validator 2000s Digi Dataloggers RH/CO2 Sensors Thermocouples Pressure Transducers HTR, LTR, CTR & Hart Baths Validation and Equipment Rentals 6 888-433-MASY (6279) www.masy.com Full Day Extended Education Class Wednesday, March 25, 2009 Risk Based Validation Class LOCATION: Biogen Idec Nobel Facility 5200 Research Place (UTC Area), San Diego, CA 92122 Program Managers: Dan Cooper Audrey Prosser, QA Manager, Mentor Corporation (J&J) s: Sponsor tics Inc. ly a Ana es, Inc. r t l U s Hach echnologi ologie n h T c M e RC ng T Buildi s n e Siem Hosted by: Jerry Yaddgo, Facilities Engineer, Biogen Idec 8:00 am - 5:00 pm Continental Breakfast and Lunch Provided To Join ISPE On-Line, Visit www.ispe.org Sponsorships are available. Please email [email protected] to inquire. REGISTRATION RISK BASED VALIDATION CLASS - March 25, 2009 To register, complete this form with credit card payment and fax it to 949-266-8461 or 949-387-9047. If paying by check, first fax your registration form then mail your check made payable to: ISPE SAN DIEGO CHAPTER, 5319 University Dr., Suite 641, Irvine, CA 92612. Chapter Hotline (800) 869-9621 or (949) 387-9046. Cancellations must be received in writing by March 18, 2009 for refund. After the cancellation date if you have reserved a space but do not attend, your payment MUST be remitted, however, an alternate person may attend in your place. If the alternate is not a member, they will need to join. Receipts for payment and Name Badges will be given at the on-site registration desk. COST ❑ $225 ISPE Members ❑ $315 NonMembers ISPE Member: Chapter Affiliation: First Name: Last Name: CREDIT CARD PAYMENT Title: Company: Address: Type of Credit Card Circle One City: Name on Card: State: Zip: Credit Card #: Tel Number: Exp Date: Fax Number: Signature: E-Mail: Save the Date On April 16th the ISPE SD Chapter is planning an evening meeting at Genentech. The topic “Lean Manufacturing and Six Sigma” is being planned by Carl Hixon of Genentech and Steven Chung of Dynalectric. The speaker is Gary Higganbotham of Solar Turbines. The presentation will include a presentation of how Genentech is incorporating Lean Manufacturing and Six Sigma into their operations. More information will be available soon and will be sent via email. www.ISPE.org/onlinelearning ® Life Sciences Group Life Sciences Group S T E RNeed I S ® Knowledge? S T E for R I STravel? Southern California Southern California No Budget 800-989-7575 www.steris.com 800-989-7575 www.steris.com No Problem. STERIS Corporation STERIS Corporation Stacey Betts ISPE Online Consumables Learning delivers critical knowledge and training to you anywhere, and Ext.anytime, 23218 at a price [email protected] fit your budget. David J. Spencer Equipment Ext. 23178 [email protected] Learn more at www.ISPE.org/onlinelearning or call Stacey Betts Consumables Ext. 23218 [email protected] David J. Spencer Equipment Ext. 23178 [email protected] ISPE Member Services at tel: +1-813-960-2105. STERIS ® STERIS Corporation STERIS Life Sciences Group Southern California 800-989-7575 www.steris.com ® STERIS Corporation Stacey Betts Consumables Ext. 23218 [email protected] David J. Spencer Equipment Ext. 23178 [email protected] Julie Lees Regional Manager, Southern CA Life Sciences Group Southern California 800-989-7575 www.steris.com Stacey Betts Consumables Ext. 23218 [email protected] David J. Spencer 619.395.3748 cell Equipment [email protected] 23178 www.hyde-ec.com [email protected] ® STERIS ® STERIS Life Sciences Group Southern California 800-989-7575 www.steris.com Christy Pavano STERIS Corporation Stacey Betts STERIS Corporation [email protected] Consumables Ext. 23218 Phone: 760-496-7091 Cell: 760-685-6232 [email protected] www.crbusa.com www.crbbuilders.com David J. Spencer n QUALIFICATION CONSULTING n DESIGN n CONSTRUCTION n COMMISSIONING Equipment Ext. 23178 [email protected] ® 8 Life Sciences Group Southern California 800-989-7575 www.steris.com Stacey Betts Consumables Ext. 23218 [email protected] David J. Spencer Equipment Ext. 23178 [email protected] ISPE San Diego & Los Angeles Chapters Present the 4th Annual Spring Golf Tournament Friday, May 1, 2009 La Costa Resort and Spa South Course http://www.lacosta.com/golf/courses-southx.asp 2100 Costa Del Mar Road, Carlsbad, CA 92009 • 800.854.5000 7:00 am 8:00 am REGISTRATION SHOT GUN START Proper Golf Attire Required No Metal Spikes 2-Person Best Ball There is a limit on the number of players Participation will be based on order paid Cost Per Player: $175 Price Includes: Green fee, Cart, Range Balls and Meal at the turn For Sponsorship Opportunities, Please contact Albert Marquez at 760-408-6081 • No handicaps • Callaway format • No door prizes • No longest drive/closest to the pin • Boxed meal will be included • Meet in bar after tournament for socializing and a cash bar Spots can be confirmed once payment is received Below is a link to our online processing site: http://event-confirmation.com/ispesd_meetings.htm Call 888-275-0189 or 949-387-9046 with any questions ISPE San Diego & Los Angeles Chapters Present the 4th Annual Spring Golf Tournament Friday, May 1, 2009 La Costa Resort and Spa South Course http://www.lacosta.com/golf/courses-southx.asp 2100 Costa Del Mar Road, Carlsbad, CA 92009 • 800.854.5000 7:00 am 8:00 am REGISTRATION SHOT GUN START REGISTRATION ISPE SD/LA Joint Golf Tournament May 1, 2009 To register, complete this form with credit card payment and fax it to 949-266-8461 or 949-387-9047. If paying by check, send your check made payable to: ISPE SAN DIEGO CHAPTER, 5319 University Dr., Suite 641, Irvine, CA 92612. Chapter Hotline (800) 869-9621 or (949) 387-9046. Sorry, no refunds for Golf Tournaments. For an immediate receipt, please use our on-line registration system: http://event-confirmation.com/ispesd_meetings.htm ❑ $175 Per Player x _______ Players = $_____________ Coordinator Name: Company: Address: City: State: Zip: Phone: Type of Credit Card Circle One Fax: E-Mail: Player Player Player Player CREDIT CARD PAYMENT Name on Card: 1: 2: 3: 4: Credit Card #: Exp Date: Signature: WELCOME NEW CHAPTER MEMBERS October 2008 - February 2009 James Anthony, Director, Enterey, Inc. Judy Atanackovic, Validation Specialist IV, Gen-Probe Jason Bakke, Division Mgr Special Projects/Interiors, Turner Construction Company Erin Bala, Inside Sales Representative, San Diego Fluid System Technologies Larry Bestmann, Sr Validation Engineer, Beckman-Coulter Rachel Dean, Student, UC Berkeley Dan Dorsey, Recruiter, R&D Partners Hassan Farah, Student, California State University Dominguez Hills Bruce Firestone, Allergan Inc Abigail Freeman, Student, Northeastern University Jon Haigis, Head of Capital Projects, Genzyme Huilan Han, Student, University of California-Davis Denise Houchens, Project Manager, Genentech Ben Huey, Engineer II, Baxter BioScience Robert Inouye, Principal Engineer, Baxter BioScience Terry James, Operations Manager, Kinetic Systems Inc Kavya Katipally, Student, University of California-Davis Eric Ketelhut, Validation Engineer, Commissioning Agents Inc. Wan-Chu Kung, Miramar Community College Karen Leung, Graduate Student, University of California-Davis Roman Levytskyy, PhD Candidate, San Diego State University Cliff Lipman, President, Coceri Jumpei Nagano, Student, University of California-Davis Noel Nevers, Project Manager, Hyde Engineering + Consulting, Inc. Stephen Nguyen, Principal Validation Engineer, Abbott Vascular Stepheni Norton, Global Software Validation Lead, DJO Global Michael O’Shea, Validation Manager, Genentech, Inc Heather Palko, Graduate Student, University of California-Davis Steve Panico, Account Manager, Emcor Service/ Mesa Energy Systems Tim Pettay, Sr. Validation Engineer, Beckman Coulter John Pinion, Sr VP, Quality & Compliance, Genentech, Inc Laura Power, Student, University of California-Davis Gary Primes, V.P. Operations, PURE Bioscience Jidong Qu, Manufacturing Engineer, Allergan Ian Schomer, VP of Corporate Development, 360 Vantage SethSchreiner, Electronic Control Systems, Inc. Debbie Stowe, System Admin, Nexgen Pharma Liban Telahun, Mechanical Engineer, CRB Kevin Tsui, Quality Engineer, Neutrogena Corp/Johnson & Johnson Evelyn Wang, Automation Engineer, Genentech Inc Willie Wells, Student, San Jose State University Jessica Zittere, QA Validation Specialist, Bayer Tech 3URFHVV+4,QF %LRSKDUPDFHXWLFDO3URFHVV6\VWHPVDQG&RPSRQHQWV $VKOHH8MLIXVD 11 67ZLQ2DNV9DOOH\5G 6DQ0DUFRV&$ WHO FHOO ID[ DVKOHH#SURFHVVKTFRP ZZZSURFHVVKTFRP O Oktoberfest Overview by Ashlee Ujifusa of BioTek Systems/ProcessHQ, Inc. n October 17, 2008 directly following a very informative and interesting bio-processing class, we had Oktoberfest at Yogi’s in Cardiff. We had 22 people attend, we all enjoyed drinks and delicious appetizers, played pool and then had a small celebration for Kimberly Syre for her birthday. Yogi’s was a great venue and their management team was so friendly and accommodating. Thank you to every one who was able to attend - we had a lot of fun! We look forward to the next social event! ISPE San Diego Chapter Board of Directors President Andy Darragh, Vice President, Ferguson Pape Baldwin Architects Vice President Don Holden, Sr. Electrical Designer, CRB Consulting Engineers PHONE EMAIL (619) 231-0751 [email protected] (760) 496-3714 [email protected] Treasurer Christy Pavano, West Reg Dir Bus Devel, CRB Engineers/Builders (760) 496-7091 [email protected] Secretary Daniel Cooper [email protected] Director Steven Chung, Control Systems Engineer, Dynalectric San Diego (858) 712-4723 [email protected] Director Laura Ellery, Account Executive, Siemens Building Technologies (858) 693-8711 [email protected] Director Mike Fino, Professor, MiraCosta College (760) 757-2121 [email protected] Director Carl Hixon, Senior Engineer, Genentech (760) 231-2819 [email protected] Director Tim Price, Process Engineer, X-nth (858) 597-0555 [email protected] Director Stacy Sutton, As’t Dir, Infrastructure/Logistics, Althea Technologies (858) 882-0123 [email protected] Director Ashlee Ujifusa, Field Sales Representative, ProcessHQ (760) 730-9376 [email protected] Director Jerry Yaddgo, Sr. Facilities Engineer, Biogen Idec, Inc. (858) 401-8062 [email protected] Past President Edward Domanico, Director of Engineering, Vical Incorporated (858) 646-1329 [email protected] 12 Energy Optimization Workshop and Facility Tour of Genentech by Carl Hixon of Genentech G enentech opened their huge doors to us once again on November 6 by hosting a facility tour and workshop. We began in the afternoon with a workshop on Energy Optimization led by Eric Nyenhuis and Pete Myers of Siemens Building Technologies. Many companies are realizing the value of energy optimization efforts and our speakers discussed their recent experience with implementing sophisticated control solutions such as VAVPlus and demand response in order to help companies save substantial operating costs and meet their sustainability goals. Christoph Lebl of Genentech gave an overview of the campus facilities before heading out on several guided tours of the utility spine and manufacturing buildings. A huge spread of food and drinks were served by the Genentech folks on their elegant café patio for attendees to enjoy before and after their tour. We always appreciate the hospitality of our member companies and Genentech pulls out all the stops! Thanks to our sponsors Dynalectric, Veriteq Instruments and Siemens Building Technologies. And thanks to our Program Managers, Carl Hixon of Genentech and Mike Barbera of Project Management Advisors for organizing this successful event. 13 January Social Event Photos Bowling at East Village Tavern + Bowl High Purity Liquid Handling Products for Pharmaceutical & Biotech Industries 1-800-726-4835 Chris Ballew Technical Sales Representative (805) 906-1533 Cell [email protected] www.sani-techwest.com 321 Irving Dr., Oxnard, CA 93030 ROD LEAVITT Leavitt-Pacific Corp. Representatives 14 1361 High Street Tel: 510-865-1655 e-mail: [email protected] Alameda, CA 94501 FAX 510-865-0979 web: www.sharpemixers.com MiraCosta Hands-On Bioprocessing Day Overview by Mike Fino of MiraCosta College O n October 17th, 2008, MiraCosta College hosted a Hands-On Bioprocessing Day. The event was held at the Biotechnology Training Facility on the Oceanside campus. The facility was designed by ISPE Members and was opened for classes in January 2006. The 3,500-square foot facility maintains over $1-million in state-of-the-art equipment, underscoring the hands-on approach MiraCosta has taken to train highly qualified technicians for the local biotechnology industry. Seventeen people participated in the event. The course was modeled after MiraCosta’s BTEC221 class, Bioprocessing: Cell Culture and Scale-Up, which is part of a program recognized by the United States Department of Labor as a National Center of Excellence. The event was coordinated and led by board member and MiraCosta faculty, Mike Fino. Nova Biomedical co-sponsored the event and provided valuable reagents for the analysis of media composition. The agenda for the day featured a mix of lecture and lab activities focused on the upstream processing activities involved in the production of a modern biopharmaceutical. Major topics for the lecture portion included an overview of large scale bioprocessing, a review of GMP-compliant documentation, common expression systems, an introduction to cell culture theory, aseptic processing, cell nutrient requirements and media design, and an introduction to process-controlled bioreactors. The lecture portions were interspersed with hands-on lab activities. The group was divided into five teams and each group was given a 500-mL spinner flask of Chinese hamster ovary (CHO) cells recombinant for a human clot-busting blood protein (tissue plasminogen activator, tPA), media components, and a 3-L bioreactor to assemble and sterilize. Each group worked against provided standard operating procedures (SOPs) and batch production records (BPRs). The groups aseptically sampled their spinner flasks to quantify their viable cell numbers and analyze the culture media. They then formulated the appropriate volume of media based on the results of their cell counts. They finished the morning session by assembling, performing initial probe calibrations, and sterilizing their own bioreactors. After lunch, the groups combined their reactors, cells, and media to start the batch production of tPA. The reactors were connected to DeltaV process-controlled bioreactor systems and all the process instrumentation was calibrated. After the setpoints and limits were established for all the process variables (temperature, pH, DO, agitation), the systems were placed into fully automated control mode. A final sample was taken to check the cell counts and process chemistries (pH, glutamine, glucose, lactate, ammonia, and osmolality). (continued on next page) 15 MiraCosta Hands-On Bioprocessing Day Overview by Mike Fino of MiraCosta College (continued) Documentation was finalized and the attendees left with a complete, hands-on experience of starting up a bioreactor culture of recombinant mammalian cells. Though their experience ended with the inoculation of the culture, the MiraCosta program kept the reactors running to produce more tPA to be used as part of their Bioprocessing Program and, specifically, the BTEC222 class, Bioprocessing: Large Scale Purifications, that started the following week. The work of the ISPE Members ultimately benefitted the students in the program and we are pleased to note that none of the cultures showed any signs of contamination at the harvest and the class was able to purify active tPA by the end of the BTEC222 class! MiraCosta College will host another Hands-On Bioprocessing Day on October 15th, 2009. This second event will focus on downstream processing and will feature a similar format of lecture and lab where attendees will work through various filtration and chromatography steps to purify the recombinant protein product expressed in the prior upstream process. For more information about the MiraCosta Biotechnology Program, please visit the program website at www.miracosta.edu/biotech. 16 ISPE Event Calendar Theme for 2009 ISPE San Diego Chapter Efficiency: Doing More With Less ISPE SAN DIEGO CHAPTER 5319 University Dr., Suite 641 Irvine, CA 92612 Chapter Hot Line: (800) 869-9621 or (949) 387-9046 -------------------Fax: (949) 387-9047 or (949) 266-8461 For advertising information: www.ispe.org/SanDiego _______________________ ISPE is a global, not-for-profit membership organization that provides education, training, and technical publications to pharmaceutical manufacturing professionals. Join ISPE Today For Great Membership Benefits: • Member Only Events/Facility Tours • Discounts to Educational Programs and Technical Documents • Subscription to Pharmaceutical Engineering magazine, with access to on-line article archives • Connection to more than 25,000 Members from 90 countries through an on-line Membership Directory and More! PHOTO CREDITS Cover Photo from fotolia.com: by photographer Armin Sepp Other Photos Christy Pavano, CRB Ashlee Ujifusa, ProcessHQ Kimberly Syre, Attention To Detail 17 17-19 March INTERPHEX, New York, NY www.interphex.com 25 March Full Day Risk Based Validation Class at Biogen Idec 1 April ISPE San Francisco/Bay Area Vendor Night South San Francisco Conference Center 7 April Advanced Cell Culture Short Course BTEC201, MiraCosta College More information, including course flyers, can be found at: www.miracosta.edu/biotech 16 April Dinner Meeting at Genentech “Lean Manufacturing & Six Sigma” 1 May Spring Golf Tournament La Costa Resort & Spa in Carlsbad 14 May ISPE LA Chapter Vendor Night Hilton Costa Mesa 1-4 June ISPE Washington Conference 18 June Evening Event 21 July Padre Game Social Event vs Florida Marlins August Vendor Night and Golf Tournament 24 September Full Day Automation Class 15 October Full Day Bioprocessing Class at MiraCosta College 15 October Oktoberfest 8-12 Nov ISPE Annual Meeting in San Diego!!! All events subject to change due to availability of venue/speakers. To Register for Any ISPE SD Meetings: http://event-confirmation.com/ispesd_meetings.htm Chapter Web site: www.ispe.org/sandiego ISPE’s Global Calendar and Additional ISPE Educational Offerings and Publications: www.ispe.org
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