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Testimonials
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Speaker is very knowledgeable. Glimpses "behind the curtain" in to the FDA are quite valuable in my opinion. ComplianceOnline has a broad catalog of professional advancement opportunities.
Manager, Quality Control, Quanterix Corporation -
The seminar was very informative for the cGMP course over multiple areas (drug, device and food). The open forum for questions and discussions was very valuable. Registration process for the seminar with ComplianceOnline was easy. Details of the course content were helpful. There was quick communication of required materials from ComplianceOnline after the registration.
Quality Assurance Coordinator, Procter & Gamble -
This seminar had a lot of excellent and useful information which will be beneficial for achieving compliance in our organization quality program. ComplianceOnline is very good at communicating and working with me.
Quality & Safety Compliance Manager, Alaffia -
Speaker was very informative, interesting and nice. All topics were important to me. Nice hotel and I was happy I had a copy of slides prior to make notes on.
Research & Development, Estée Lauder Companies -
The instructor was very knowledgeable and lab auditing topic was most valuable to me.
Food Safety and Quality Coordinator, The Raymond-Hadley Corporation -
Great experience, very valuable. The instructor gave lot of great examples.
Sr. Director QC, Hologic Gen-Probe -
I really enjoyed this conference as I am new to the regenerative medical space & found this was a great source to get up to speed on how FDA is currently reviewing this space.
Associate Product Manager, Zimmer Biomet
Key Areas:
FDA Audits and Inspections | eCTD Submissions | FDA's GMPa Expectations | Regenerative Medicine | FDA Legal Authority | Promotion and Advertising | Stem Cell Treatments | Tissue Engineering | Gene Therapies | Off Label Use | Custom Device Promotion | Systematic Operating Procedures (SOPs) | Outsourcing Activities | First-in-Man Clinical Trials | IND Submission | Vendor Selection | Process Validation | Warning Letter | Foreign Inspections | FDA's New Import Program | FDA Recalls | CAPA
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada: 2-day In-person Seminar
San Francisco, CA | May 31-Jun 1, 2018
FDA's New Import Program for 2018 - Strict Precision: 2-Day In-Person Seminar by Ex-FDA Official
San Francisco, CA | June 21-22, 2018
Managing Your FDA Inspection: Before, During and After: 2-Day In-Person Seminar by Ex-FDA Official
San Francisco, CA | Jun 28-29, 2018
FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials: 2-Day In-Person Seminar by Ex-FDA Official
San Francisco, CA | Aug 21-22, 2018
Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half Day In-Person Seminar by Ex-FDA Official
Philadelphia, PA| Aug 30-31, 2018
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If you find same seminar on another website at a lower rate, contact our customer care team without
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