Pharmaceutical Validation – Latest Global Regulations and Trends to Stay Compliant

Date	Aug 23, 2018
Time	10:00 AM EDT
Cost	$18000.00
Online

The two day workshop on Pharmaceutical Validation – Latest Global Regulations and Trends to Stay Compliant, is designed to provide an in-depth understanding of the concept of pharmaceutical validations based on the current FDA, EU and ICH guidance documents as well as learnings from the pharmaceutical industry. Special emphasis will be laid on practical approach and simple illustrative examples from the industry for judicious and effective implementation.

OBJECTIVES:
Participants will leave the workshop with a greater understanding of:

• FDA, ICH and EU Regulations
  • Process Validation
  • Validation Master Plan
  • Equipment Qualification
  • Risk Management Tools and Techniques
  • Process Design and Development
  • Technology Transfer
  • Continuous Process Verification
  • Analytical Method Validation
  • Cleaning Validation
  • SOPs and Best Practices
  • CASE STUDIES …. and More

WHO SHOULD ATTEND:
A must attend seminar for professionals in Pharmaceuticals, QC Laboratories, Manufacturers of drug substances (APIs), Oral Solid Dosage Form, Contract Laboratories, Clinical research Organizations, Contract Research Organisations, Contract Manufacturing Organisations and Biopharma companies.

DEPARTMENTS:
– Quality Control
– Quality Assurance
– Research and Development
– Manufacturing
– Engineering
– Analytical Development Laboratories
– Regulatory Compliance
– Validation
– Production
– Technology Transfer
– Laboratory
– Documentation
– Training Departments

PROFESSIONALS:
– Managers
– Supervisors
– Senior Managers
– Team Leaders
– Executives and Senior Executives
– General Managers
– Engineers
– Design Engineers
– Plant Managers
– Laboratory Managers and Supervisors
– Regulatory Affairs Managers
– Documentation Specialists & Analysts
– Internal and External Auditors