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2011
Cosmetic/Skin Product Course
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- A Practical
Introduction to Regression Analysis
- Analytical
Method Validation for Pharmaceutical, Biopharmaceutical,
and Biologics Quality Control
- Aseptic
Processing in the Manufacture of Biotech and Pharmaceutical
Products
- Biostatistics
for Non-Statisticians
- cGMP for
Quality Assurance and Quality Control of Pharmaceuticals,
Biopharmaceuticals, and Biologics
- Comprehensive
Overview of FDA Regulatory Compliance for Drugs and
Biotech Products
- Core Skills
for Team Development
- Current
Good Laboratory Practices & Current Good Manufacturing
Practices - A Basic Primer
- Dermatological
Product Development
- Effective
Document Management for the Pharmaceutical, Biotech
& Medical Device Industries
- Effective
Quality Assurance Auditing for FDA Regulated Industries
- Effective
Risk-Based Applications of cGMPs for Cosmetics and OTC
Drug Products
- European
Filing & Registration Procedures
- FDA Inspections
of Clinical Data Systems
- FDA Inspections:
What To Expect And How To Prepare
- Financial
Fundamentals for Non-Financial Personnel - How Financial
Issues Impact Business
- Good Clinical
Practices (GCPs)
- How to Implement
Risk Management Principles and Activities Within a Quality
Management System
- How to Monitor
Clinical Trials for GCP Compliance
- How to Prepare
for a Systems-based Inspection – Understanding
the FDA’s Risk-based Inspections Approach and
Ensuring Compliance
- Introduction
to Effective Medical Writing
- Introduction
to Statistical Analysis of Laboratory Data
- Laboratory
Safety - Basics and Beyond
- Management,
Supervisory & Leadership Skills for R&D Personnel
- Moving from
Discovery Into Development
- Outsourcing
for the Therapeutic Products Industry
- Outsourcing
Preclinical Toxicology Studies
- Overview
Of FDA Regulatory Compliance For Medical Devices
- Pharmaceutical
Counterfeits and Intellectual Property Rights Infringement
in China
- Pharmaceutical
Water Systems: Contemporary Technology and Compliance
- Pharmaceutical,
Biopharmaceutical, and Biologics Quality Control Laboratories:
A Regulatory Compliance Primer
- Practical
Methods for Project Management
- Project
Management for Phase 1 & 2 Clinical Trials
- Project
Management for the Phase 3 and LCM (Life Cycle Management)
of the Drug Development Process
- Root Cause
Analysis for CAPA
- Safety Pharmacology
in Drug Development
- Skin Product
Development
- Sterilization
Procedures: Technology, Equipment and Validation
- Technical
Writing for the Pharmaceutical, Medical Device, and
Biotech Industries
- The Drug
Development Process - From Discovery to Commercialization
Validation of Computer Systems
- Writing
Effective Standard Operating Procedures and Other Process
Documents
Writing in the Regulated Environment When English Is
Your Second Language
Copyright
© 1996-2011 Yale Pharmaceutical
Research Institute |
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