About Us

Are you getting the most of your current CAPA system? Eminence Business Media's "Improving Investigation Process & CAPA 2018" answers this question and also teaches you how to tackle the toughest CAPA challenges including how to shorten & better manage CAPA investigations  thus improving product quality & ensuring compliance.

Who will Attend?

All the delegates attending are carefully screened and selected to meet specific criteria with regard to job level, the scope of responsibility and investment portfolio to ensure the highest quality for all those attending. The results of our selection process ensure an attendee list consisting of senior decision-makers from the industry.


Managing Directors, Presidents, Sr. VP's, VP's, Sr. Directors, Directors, Site / Plant Heads, General Managers, Sr. Managers, Managers.


* Quality Assurance

* Quality Control

* Regulatory

* Manufacturing

* Production

* Engineering

Key Highlights / USP


Learn from a seasoned USFDA Consultant


Trainer with 30+ years of hands on CAPA Experience

Case Studies

Interactive Case Studies / Exercises


Dedicated Q&A Sessions


A pool of networking opportunities


Dr. George Bernstein

Principal, Double Dragon Consulting, Inc. & USFDA Consultant

George Bernstein, Ph.D., has been a USFDA Consultant on CAPA, Root Cause analysis and GLP. He is also the Principal with Double Dragon Consulting, Inc., a consulting firm with a network of Subject Matter Experts (SMEs) located in the US, Europe, and Asia Pacific (China, India).


Dr. Bernstein has a Ph.D. in Chemical Engineering and over 30 years of experience in pharmaceutical manufacturing, laboratory operations, data integrity, effective training, and quality risk management.


Since 1988, Dr. Bernstein has consulted internationally with major pharmaceutical companies. He has lectured on quality systems and root cause analysis to industry trade groups, quality organizations, and at Interphex.


Dr. Bernstein’s experience, insights, and innovative problem solving have been integral to his work which ranges from GMP compliance, facility design, construction, and commissioning to business process re-engineering and process optimization. He has developed global quality standards (GLP, GCP, GPP) for a major international pharmaceutical company, and has assisted many clients with audit preparation, remediation activities, and communications with the US FDA.


He recently authored the following articles on LinkedIn:


“FDA and Data Integrity – 3 Perspectives”


“API Manufacturing and Data Integrity – an Auditor’s Perspective”


Dr. Udaykumar Rakibe

Dr. Udaykumar Rakibe

Founder PharmaMantra & Former Sr. VP, Wockhardt

Dr. Varada Bapat

Dr. Varada Bapat

Associate Vice President - Wockhardt

Dr. Ranjit Barshikar

Dr. Ranjit Barshikar

Quality Management Consultant

Mr. Sanjay Jangir

Mr. Sanjay Jangir

DGM - Quality Systems, Sunpharma

Mr. Vikam Pundir

Mr. Vikam Pundir

Site Quality Head, Novartis

Mr. Manmeet Singh

Mr. Manmeet Singh

General Manager, Sunpharma

Event Partners

Gold Partner
Knowledge Partners
Media Partners

Pricings to attend

First 35


INR 26000 + GST = INR 30680



USD 650 + GST = USD 767

Next 45


INR 30000 + GST = INR 35400



USD 750 + GST = USD 885

Next 50


INR 34000 + GST = INR 40120



USD 850 + GST = USD 1003


The registration for Improving Investigation Process & CAPA 2018 is closed now.

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Hotel Sahara Star, Mumbai Suburban, Maharashtra, India, 400099

We would love to hear from you.

For Speaking Opportunities

Roshni Verma
022 4972 4927

For Sponsorship Opportunities

Viral Bhatt
022 4972 4927

For Delegate Registrations

Suryansh Rana
+91 9653 284 123 | 022 4972 49