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Introduction to Biotechnology Analytical Methods

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This webinar will highlight the evidence normally requested during audits and inspections of biotechnology analytical labs. You will learn how your laboratory's biotechnology analytical methods can fulfill stated or implied regulatory requirements (the US FDA refers to these as the “C” in CGMPs).

Speaker
Instructor: Robert D Seltzer
Product ID: 702481

Why Should You Attend:

You should attend this webinar if:

  1. You are a full-time compliance and quality auditor
  2. you may be called upon to assist one or a team of auditors going into your own company’s or a contracted quality control lab for biotechnology analyses
  3. you may be called upon to perform a department self-inspection
  4. you may be a member of the biotechnology/biochemistry analytical laboratory supervision or management who will host future audits and regulatory inspections

This webinar will show how GMP compliance and good science intersect in this critical laboratory supporting biotechnology API and the resulting, finished pharmaceutical manufacturing. This session will shed light on the evidence normally requested during audits and inspections of biotechnology analytical labs. You will learn how an FDA auditor/inspector thinks and use that knowledge to help your microbiology laboratory and its equipment, documents, records, personnel, etc. become audit-friendly.

Areas Covered in the Seminar:

Who Will Benefit:

This webinar will provide auditing tools as well as useful compliance knowledge and ideas for continual improvement to the following individuals inside and outside the life sciences industries:

Instructor Profile:

Bob Seltzer, has more than 25 years in R&D, Process Development, and Quality Assurance/Compliance in pharmaceuticals, medical devices, food, dietary supplements, and cosmetics industries. He is currently President and Principal Consultant of "Worldwide GMP Compliance Professional (WWGMPCP)," providing due diligence, quality and compliance, and supplier auditing, risk management, consulting, technical writing, and training in domestic or international pharmaceutical, medical device, food, dietary supplement, and/or cosmetic Good Manufacturing Practices and related regulations, guidances, standards, compendia/monographs. He holds an M.S., Biochemistry; B.S., Chemical Engineering; and B.A., Biochemistry, all from Rutgers, New Brunswick. He is an ASQ Certified Quality Auditor, Quality Engineer, Manager of Quality/Organizational Excellence, Biomedical Auditor, and holds certificate No. 1 in the Certified Pharmaceutical GMP Professional after having founded and championed that certification adopted by the American Society for Quality in 2008.

Topic Background:

The end-product of biotechnological manufacturing is a protein. Proteins are relatively large molecules (between 2 kDaltons and 800 kDaltons). Their functionality (measurable as activity) depends on an intact three-dimensional structure. Activity assays must complement protein concentration (quantity) assays to determine the purity and potency of the protein of interest during manufacturing purification processes. An inactivated or denatured protein is completely non-potent, regardless of its concentration/quantity.

The analytical methods associated with manufacturing a protein via recombinant DNA technology (i.e., using genetically-modified bacteria or fungi or mammalian cells) are (i) protein and nucleic acid biochemical quantitation and characterization tests as well as (ii) tests for adventitious (i.e., unintended contaminating) organisms such as viruses and mycoplasma.

The auditing skills called upon when assessing biotechnology analytical methods, laboratories, equipment, instruments, and personnel are distinct from the science that underlies biochemistry/biotechnology. In other words, the mindset, background/experience, and intuition of a biochemistry/biotechnology analyst are alone insufficient for performing effective audits of these laboratories and analyses. Instead, holistic GMP compliance knowledge and experience and properly comprehensive audit planning and organization are necessary and sufficient for fulfilling the regulatory inspectorate’s expectations of this highly important combination compliance-and-quality audit.

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Refund Policy
"Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance.
ComplianceOnline would process/provide refund only if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs."
For substitution, please email editor@complianceonline.com or call +1-650-620-3937.

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Training Options Training Duration = 75 Min
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