Biopharmaceutical & Pharmaceutical Training & Technology, Medical Device & Biotech Training - CfPIE
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Click on one of links below to find the Biotech, Medical Device, Skin/Cosmetic or Pharmaceutical training course that best fits your schedule.
September, 2010
 
Sep. 08 - 10, 2010Introduction to Molecular Biology Techniques – Applications in the Biotechnology and Pharmaceutical Industries
Sep. 08 - 10, 2010Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
Sep. 09 & 10, 2010Preparing the CMC Section for NDAs/INDs/CTDs
Sep. 15 - 17, 2010ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
Sep. 15 & 16, 2010Financial Fundamentals for Non-Financial Personnel - How Financial Issues Impact Business
Sep. 15 & 16, 2010Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
Sep. 16 & 17, 2010Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Sep. 20 - 22, 2010CMC Regulatory Compliance for Biopharmaceuticals and Biologics
Sep. 20 & 21, 2010Clinical Document Management - A Trial-by-Trial Approach to Compliance
Sep. 20 & 21, 2010Labeling and Labeling Controls in the Medical Device Industry
Sep. 20 & 21, 2010Validation of Computer Systems
Sep. 21 & 22, 2010Introduction to Medical Device Submissions – 510ks, PMAs, and Exemptions
Sep. 21 & 22, 2010Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
Sep. 22 - 24, 2010Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
Sep. 23 & 24, 2010Best Practices for Facilities and Utilities Design, Qualification and Monitoring – Applying the Life-Cycle Concept
Sep. 23 & 24, 2010Introduction to Medical Combination Products
Sep. 23 & 24, 2010Stability Programs for Product Shelf Life – From Development to Approval
Sep. 27 & 28, 2010Adverse Drug Events – Reporting & Regulatory Requirements
Sep. 27 & 28, 2010Best Practices for an Effective Cleaning Validation Program
Sep. 27 & 28, 2010Design Control for Medical Device Professionals
Sep. 27 & 28, 2010Good Laboratory Practices (GLP) for Pre-Clinical Testing
Sep. 27 & 28, 2010Writing Effective Standard Operating Procedures and Other Process Documents
Sep. 28 & 29, 2010The EU Clinical Trial Directive
Sep. 29 - Oct. 1, 2010Good Manufacturing Practices (cGMP)
Sep. 29 - Oct. 1, 2010The Drug Development Process - From Discovery to Commercialization
Sep. 29 & 30, 2010Design Validation, Verification, and Risk Analysis for Medical Device Professionals
Sep. 29 & 30, 2010Process Validation for Drugs and Biologics
Sep. 30 & Oct. 01, 2010Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
Sep. 30 & Oct. 01, 2010European Filing & Registration Procedures
 
October, 2010
 
Oct. 04 - 06, 2010Tablets and Capsules - Development, Manufacture and Testing of Solid Oral Dosage Forms
Oct. 04 & 05, 2010Patent and Other Intellectual Property Law for the Life Sciences Industry
Oct. 04 & 05, 2010Practical Methods for Project Management
Oct. 04 & 05, 2010Validation of Computer Systems
Oct. 05 & 06, 2010Effective Quality Assurance Auditing for FDA Regulated Industries
Oct. 05 & 06, 2010The EU Clinical Trial Directive
Oct. 07 & 08, 2010Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
Oct. 07 & 08, 2010European Filing & Registration Procedures
Oct. 07 & 08, 2010How to Implement Risk Management Principles and Activities Within a Quality Management System
Oct. 07 & 08, 2010Quality System Regulation for the Medical Device & Biotech Industries
Oct. 11 & 12, 2010FDA Inspections: What To Expect And How To Prepare
Oct. 11 & 12, 2010How to Monitor Clinical Trials for GCP Compliance
Oct. 11 & 12, 2010Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
Oct. 12 & 13, 2010Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
Oct. 13 - 15, 2010Process Validation for Medical Devices
Oct. 13 - 15, 2010QA/QC Strategy for Biologics and Biopharmaceuticals
Oct. 13 & 14, 2010Detecting Fraud and Misconduct in Clinical Trials
Oct. 14 & 15, 2010Pharmaceutical Production Batch Record Review
Oct. 18 - 20, 2010Biostatistics for Non-Statisticians
Oct. 18 & 19, 2010Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Oct. 20 - 22, 2010CMC Regulatory Compliance for Biopharmaceuticals and Biologics
Oct. 21 & 22, 2010Auditing and Qualifying Suppliers and Vendors – An Effective Risk Based Approach
Oct. 21 & 22, 2010Essentials of Program, Project & Portfolio Management in Bio-Pharmaceutical Discovery
Oct. 21 & 22, 2010Introduction to Statistical Analysis of Laboratory Data
Oct. 25 & 26, 2010Best Practices for an Effective Cleaning Validation Program
Oct. 25 & 26, 2010Design Control for Medical Device Professionals
Oct. 25 & 26, 2010Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
Oct. 27 & 28, 2010Design Validation, Verification, and Risk Analysis for Medical Device Professionals
Oct. 27 & 28, 2010Process Validation for Drugs and Biologics
Oct. 28 & 29, 2010FDA Inspections of Clinical Data Systems
Oct. 28 & 29, 2010Introduction to Effective Medical Writing
 
November, 2010
 
Nov. 01 & 02, 2010Project Management for Phase 1 & 2 Clinical Trials
Nov. 02 & 03, 2010Selecting and Managing CROs
Nov. 03 - 05, 2010Spectroscopic Method Development for the Pharmaceutical & Biotech Industries
Nov. 03 & 04, 2010Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
Nov. 04 & 05, 2010Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
Nov. 04 & 05, 2010Effective Laboratory Safety Management
Nov. 08 & 09, 2010Cleanroom Microbiology for the Non-Microbiologist
Nov. 10 - 12, 2010The Drug Development Process - From Discovery to Commercialization
Nov. 10 & 11, 2010Sterilization Procedures: Technology, Equipment and Validation
Nov. 11 & 12, 2010Preparing the CMC Section for NDAs/INDs/CTDs
Nov. 15 - 17, 2010Good Clinical Practices (GCPs)
Nov. 15 & 16, 2010Latin America – Understanding Regulatory Compliance Requirements
Nov. 16 & 17, 2010Pharmaceutical Water Systems: Contemporary Technology and Compliance
Nov. 16 & 17, 2010Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
Nov. 17 & 18, 2010Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Nov. 18 & 19, 2010Effective Risk-Based Applications of Drug cGMPs and Validation Req. for Cosmetics and OTC Drug Prod.
Nov. 30 & Dec. 01, 2010Selecting and Managing CROs
 
December, 2010
 
Dec. 01 - 03, 2010Good Manufacturing Practices (cGMP)
Dec. 01 - 03, 2010Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
Dec. 02 & 03, 2010Clinical Trial Design For Medical Devices
Dec. 02 & 03, 2010Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
Dec. 06 - 08, 2010cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
Dec. 06 & 07, 2010Validation of Computer Systems
Dec. 13 & 14, 2010Good Clinical Practice for Medical Device Investigations
Dec. 15 & 16, 2010Good Clinical Practice Auditing
 


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