GRC Seminars | Online Regulatory Compliance Training | FDA Regulations Training, GRC Consulting, Best Practices, Standards and News

Season

Fall
Winter
Spring
Summer

Region

USA (East Coast)
USA (West Coast)
USA (Mid-West)
USA (North-East)
USA (South-East)
USA (South-West)
Africa
Asia
Australia
Europe
Middle East
South America

Areas of interest

All FDA Regulated Functions
Banking & Financial Services
Clinical Research
Corporate Governance
Drugs and Chemicals
FDA 21 CFR Part 11
FDA Validation
Financial Services and Trading
Food Safety Compliance
Healthcare Compliance
HIPAA/HITECH
HR Compliance
Laboratory
Life Sciences
Medical Devices
OSHA Compliance
Risk Management
Testing and Validation
Trade And Logistics Compliance

Industry

City

Country

Month

Upcoming Seminars

PV (Pharmacovigilance) Audit Strategy Planning – A Practical Approach to Design and Implementation: 2-Day In-Person Seminar
October 25-26, 2018 - San Francisco, CA
View Details | Register
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices: 2-day In-person Seminar
November 1-2, 2018 - Boston, MA
View Details | Register
Project Management in Clinical Research: 2-Day In-Person Seminar
November 1-2, 2018 - San Francisco, CA
View Details | Register
Computer System Validation – Reduce Costs and Avoid 483s: 2-day In-person Seminar
November 6-7, 2018 - San Francisco, CA
View Details | Register
21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar
November 6-7, 2018 - San Francisco, CA
View Details | Register
FDA’s New Import Program for 2018 – Strict Precision: 2-Day In-Person Seminar by Ex-FDA Official
November 8-9, 2018 - Boston, MA
View Details | Register
Supplier Management for Medical Device Manufacturers: 2-day In-person Seminar
November 8-9, 2018 - Boston, MA
View Details | Register
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment – Issues and Solutions: 2-day In-person Seminar
November 8-9, 2018 - Orlando, FL
View Details | Register
Complete 1099, TIN Matching, B-Notice, FATCA and Nonresident Alien 1042-S Compliance Update: 2-Day In-Person Seminar
November 8-9, 2018 - Columbia, SC
View Details | Register
Critical Vendor Risk Management: Exclusive One and a Half-day Boot Camp
November 8-9, 2018 - Chicago, IL
View Details | Register

Customer Support

Toll Free +1-888-771-6965
Fax +1-650-362-2367
Email Support

Seminar catalog

Testimonials

The presentation and flow was well organized and related. I like the Tolerance Intervals since they relate to single point measurements.

DPT Labs

This was a well-organized event. The speaker was very informative and the seminar covered great real life examples that kept everyone engaged. GRC Seminars is very helpful and it always has a professional approach in conducting their events.

Third Party Vendor Management LeadJPMorgan Chase

The seminar was very good and useful to my area. I like the areas covered on statistical analysis for method validation – Because I am doing lots of validation, method transfer etc. GRC Seminars is a great tool for quality organizations.

Associate DirectorPfizer

The training covered a large amount of data but moved at a good pace with lots of examples. The venue was very good and seminar was well organized by GRCSeminars.

Novartis

The seminar was very good and useful to my area. I like the areas covered on statistical analysis for method validation – Because I am doing lots of validation, method transfer etc.

Thanks for conducting this seminar, Medical Device companies always need to be compliant so guidance/updates are always needed. I would recommend GRCSeminars.com to others. Thanks!

Manager, Clinical OperationsClovis Oncology

This course was excellent. Bob is very knowledgeable and have answered all my questions. I like the knowledge delivered on Clinical, however, got a lot more on other topics as well. Good Summary. I would like to attend future seminars on China and Latin America.

Sr. Director of Regulatory AffairsSTAAR Surgical

Thank you. Your staff was very supportive, good choice of topic and content. Everything was valuable there. Thanks again!

DirectorAgile Systems and Processes

The training was excellent and I encountered no difficulties either with the registration process or during the event. This was one of the better trainings that I have attended over the years.

Sr. QA Engineer

It was a knowledgeable seminar. Thanks for inviting me. I will attend upcoming seminars on ISO 13485 and Sterilization validation.

Director of Quality

By using this site you agree to our use of cookies. Please refer to our privacy policy for more information. Close

Upcoming Seminars