PARTIAL CLIENTELE

UPCOMING SEMINARS IN INDIA

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Risk Management in Medical Devices Industry

Venue: To be Announced

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GMP for Quality Control Laboratories and FDA Audit Preparation

Venue: To be Announced

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Good Laboratory Practices (GLP)

Venue: To be Announced

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cGMP Audits and Inspections – Preparation and Readiness

Venue: To be Announced

INTERNATIONAL SEMINARS

Quality by Design for Medical Devices – Essential Techniques
- August 2 - 3 | Baltimore, USA

ICH Q11 – API Manufacturing Workshop
- August 9 - 10 | Philadelphia, USA

Auditing IT Systems for Regulatory Compliance
- August 23 - 24 | Florida, USA

21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
- September 13 - 14 | California, USA

Analytical Method Validation for Pharmaceutical Quality Control
- September 13 - 14 | Zurich, Switzerland

Technical Training for Life Sciences Industry
- September 27 - 28 | Raleigh, USA

Root Cause Analysis and CAPA
- October 25 - 26 | London, UK

TESTIMONIALS

"Excellent seminar – one of the best I have ever attended. Superior speaker who was very knowledgeable about the topic."
- Director of Quality, Glenmark

"Presentation was thought-provoking and provided practical skills to accomplish my given role. I expect to actually use this material and techniques in practice."
Sr. Manager, Cipla

"This workshop was very insightful and made absolute sense in terms of the Principles and their application. I am thankful for having the opportunity to attend."
HOD - Quality & Regulatory, Dr. Reddy's

"This workshop was a terrific use of my time. I will take so much back with me to use for myself and to better my organization."
Technical Director, AstraZeneca

"Excellent overview of the subject matter in two days. Very informative for both novice and intermediate level compliance professionals in the industry."
Quality Head, Gland Pharma

PARTNER WITH COMPLIANCE TRAININGS

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