Biopharmaceutical & Pharmaceutical Training & Technology, Medical Device & Biotech Training - CfPIE
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Cosmetic/Skin Product Course Listings

Below is our list of training programs that deal with skin, cosmetic and dermatological issues. For registration information and course descriptions, click on any title:
Active Pharmaceutical Ingredient (API) and Drug Product Specifications
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
Auditing and Qualifying Suppliers and Vendors – An Effective Risk Based Approach
Best Practices for an Effective Cleaning Validation Program
Best Practices for Facilities and Utilities Design, Qualification and Monitoring – Applying the Life-Cycle Concept
Biostatistics for Non-Statisticians
cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
Cost Contained Regulatory Compliance for the Drug, Biologics and Medical Device Industries
Dermatological Product Development
Detecting Fraud and Misconduct in Clinical Trials
Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
Effective Laboratory Safety Management
Effective Qualification and Monitoring of Processing Equipment and Their Control Systems
Effective Quality Assurance Auditing for FDA Regulated Industries
Effective Risk-Based Applications of Drug cGMPs and Validation Req. for Cosmetics and OTC Drug Prod.
Essentials of Program, Project & Portfolio Management in Bio-Pharmaceutical Discovery
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 Practice Auditing
Good Clinical Practices (GCPs)
Good Laboratory Practices (GLP) for Pre-Clinical Testing
Good Manufacturing Practices (cGMP)
How to Develop an Effective Complaint Handling and Post Market Surveillance and MDR Program for Devices
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
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Latin America – Understanding Regulatory Compliance Requirements
Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
Optimization of Drug-Like Properties in Drug Discovery – Assessment and Structure Modification Strategies
Outsourcing for the Therapeutic Products Industry
Overview Of FDA Regulatory Compliance For Medical Devices
Patent and Other Intellectual Property Law for the Life Sciences Industry
Pharmaceutical and Biopharmaceutical Quality Control Laboratories -  A Regulatory Compliance Primer
Pharmaceutical Production Batch Record Review
Pharmaceutical Water Systems: Contemporary Technology and Compliance
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
Skin Product Development
Sterilization Procedures: Technology, Equipment and Validation
Tablets and Capsules - Development, Manufacture and Testing of Solid Oral Dosage Forms
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

 

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Malvern, PA 19355
Phone: 610-688-1708