Available Courses

Results (113)




Course Title Course Date Location
Introduction to Effective Medical Writing Apr 23, 2018 - Apr 24, 2018 Malvern, PA United States
The Drug Development Process from Concept to Market Apr 23, 2018 - Apr 25, 2018 Malvern, PA United States
Water Purification Systems for Regulated Industries Apr 23, 2018 - Apr 24, 2018 Los Angeles, CA United States
Heating, Ventilation & A/C in a Regulated Environment Apr 25, 2018 - Apr 27, 2018 Los Angeles, CA United States
Technical Writing for Pharma, Biotech and Med Devices Apr 25, 2018 - Apr 27, 2018 Malvern, PA United States
Integration of Risk Management Principles and Activities into the Quality System May 14, 2018 - May 15, 2018 Malvern, PA United States
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development May 15, 2018 - May 17, 2018 Boston, MA United States
Medical Device Process Validation Training for Professionals May 16, 2018 - May 18, 2018 Malvern, PA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions May 21, 2018 - May 22, 2018 Malvern, PA United States
Preparing the CMC Section for NDAs/INDs/CTDs May 21, 2018 - May 22, 2018 Malvern, PA United States
Writing Effective SOP and Other Process Documents May 21, 2018 - May 22, 2018 Boston, MA United States
Clinical Document Management: A Trial-by-Trial Compliance Approach May 23, 2018 - May 24, 2018 Boston, MA United States
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars May 23, 2018 - May 25, 2018 Berlin, Germany
Introduction to Medical Combination Products May 23, 2018 - May 25, 2018 Malvern, PA United States
Design Control for Medical Device Professionals May 29, 2018 - May 30, 2018 Berlin, Germany
Preparing the CMC Section for MAAs-IMPDs May 30, 2018 - May 31, 2018 Berlin, Germany
Design Validation, Verification, and Risk Analysis for Medical Device Professionals May 31, 2018 - Jun 01, 2018 Berlin, Germany
Computer System Validation Jun 04, 2018 - Jun 05, 2018 Boston, MA United States
GMPs for OTC & Cosmetic Products - US and Global Requirements Jun 07, 2018 - Jun 08, 2018 Boston, MA United States
European Regulatory Procedures - EMA & National Requirements Jun 11, 2018 - Jun 12, 2018 Malvern, PA United States
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Jun 13, 2018 - Jun 15, 2018 Malvern, PA United States
Good Manufacturing Practices Training | GMP Course Jun 18, 2018 - Jun 20, 2018 Malvern, PA United States
Pharmaceutical Production Batch Record Review | Training Jun 18, 2018 - Jun 19, 2018 Malvern, PA United States
Preparation of FDA Submissions and Communicating with the FDA Jun 18, 2018 - Jun 19, 2018 Los Angeles, CA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Jun 20, 2018 - Jun 22, 2018 Malvern, PA United States
Auditing and Qualifying Suppliers and Vendors Jun 21, 2018 - Jun 22, 2018 Los Angeles, CA United States
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Jun 25, 2018 - Jun 26, 2018 Malvern, PA United States
Product Quality Reviews Jun 25, 2018 - Jun 26, 2018 Malvern, PA United States
Stability Programs for Determining Product Shelf Life Jun 25, 2018 - Jun 26, 2018 Los Angeles, CA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Jun 27, 2018 - Jun 28, 2018 Malvern, PA United States
Introduction to Statistical Analysis of Laboratory Data Jul 09, 2018 - Jul 10, 2018 Malvern, PA United States
Development & Validation of Bioanalytical Assays for Biologics? Jul 10, 2018 - Jul 11, 2018 Malvern, PA United States
Biostatistics for Non-Statisticians Jul 11, 2018 - Jul 13, 2018 Malvern, PA United States
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Jul 11, 2018 - Jul 13, 2018 Malvern, PA United States
Lyophilization Technology-Application of Scientific Principles Jul 12, 2018 - Jul 13, 2018 Boston, MA United States
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Jul 16, 2018 - Jul 17, 2018 Boston, MA United States
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Jul 16, 2018 - Jul 17, 2018 Malvern, PA United States
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer Jul 23, 2018 - Jul 24, 2018 Los Angeles, CA United States
Process Validation for Drugs and Biologics Jul 25, 2018 - Jul 26, 2018 Los Angeles, CA United States
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Jul 30, 2018 - Jul 31, 2018 Boston, MA United States
The Drug Development Process from Concept to Market Jul 30, 2018 - Aug 01, 2018 Malvern, PA United States
Understanding & Implementing New EU Clinical Trial Regulation Aug 02, 2018 - Aug 03, 2018 Malvern, PA United States
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Aug 06, 2018 - Aug 08, 2018 Los Angeles, CA United States
Medical Writing When English Is Your Second Language Aug 06, 2018 - Aug 07, 2018 Malvern, PA United States
Writing Effective SOP and Other Process Documents Aug 08, 2018 - Aug 09, 2018 Malvern, PA United States
Preparing the CMC Section for NDAs/INDs/CTDs Aug 09, 2018 - Aug 10, 2018 Boston, MA United States
Best Practices for an Effective Cleaning Validation Program Aug 13, 2018 - Aug 14, 2018 Boston, MA United States
Design Control for Medical Device Professionals Aug 13, 2018 - Aug 14, 2018 Malvern, PA United States
Introduction to Effective Medical Writing Aug 13, 2018 - Aug 14, 2018 Los Angeles, CA United States
Water Purification Systems for Regulated Industries Aug 13, 2018 - Aug 14, 2018 Malvern, PA United States
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Aug 15, 2018 - Aug 16, 2018 Malvern, PA United States
Heating, Ventilation & A/C in a Regulated Environment Aug 15, 2018 - Aug 17, 2018 Malvern, PA United States
Technical Writing for Pharma, Biotech and Med Devices Aug 15, 2018 - Aug 17, 2018 Los Angeles, CA United States
Clinical Trial Project Management, Phase 1-4 Best Practices Aug 20, 2018 - Aug 22, 2018 Boston, MA United States
Effective Document Management for Pharma, Biotech & Medical Device Aug 23, 2018 - Aug 24, 2018 Boston, MA United States
Project Management for Medical Device Product Development Sep 06, 2018 - Sep 07, 2018 Malvern, PA United States
Auditing and Qualifying Suppliers and Vendors Sep 13, 2018 - Sep 14, 2018 Malvern, PA United States
Computer System Validation Sep 13, 2018 - Sep 14, 2018 Malvern, PA United States
European Regulatory Procedures - EMA & National Requirements Sep 13, 2018 - Sep 14, 2018 Berlin, Germany
Overview of FDA Regulatory Compliance for Medical Devices Sep 17, 2018 - Sep 18, 2018 Malvern, PA United States
Specifications for APIs & Pharmaceutical Drug Products Sep 17, 2018 - Sep 18, 2018 Malvern, PA United States
Introduction to Effective Medical Writing Sep 24, 2018 - Sep 25, 2018 Berlin, Germany
Pharmaceutical Production Batch Record Review | Training Sep 24, 2018 - Sep 25, 2018 Boston, MA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Sep 26, 2018 - Sep 28, 2018 Boston, MA United States
Technical Writing for Pharma, Biotech and Med Devices Sep 26, 2018 - Sep 28, 2018 Berlin, Germany
The Drug Development Process from Concept to Market Oct 01, 2018 - Oct 03, 2018 Boston, MA United States
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Oct 02, 2018 - Oct 04, 2018 Boston, MA United States
Understanding & Implementing New EU Clinical Trial Regulation Oct 04, 2018 - Oct 05, 2018 Boston, MA United States
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Oct 09, 2018 - Oct 11, 2018 Berlin, Germany
Good Manufacturing Practices Training | GMP Course Oct 10, 2018 - Oct 12, 2018 Boston, MA United States
Introduction to Molecular Biology Techniques Oct 10, 2018 - Oct 12, 2018 Malvern, PA United States
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Oct 11, 2018 - Oct 12, 2018 Boston, MA United States
Introduction to Statistical Analysis of Laboratory Data Oct 11, 2018 - Oct 12, 2018 Boston, MA United States
Auditing and Qualifying Suppliers and Vendors Oct 15, 2018 - Oct 16, 2018 Berlin, Germany
Biostatistics for Non-Statisticians Oct 15, 2018 - Oct 17, 2018 Boston, MA United States
Selecting and Managing CROs Oct 17, 2018 - Oct 18, 2018 Boston, MA United States
Advanced Topics in Biostatistics for Non-Statisticians™ Oct 18, 2018 - Oct 19, 2018 Boston, MA United States
Clinical Trial Design For Medical Devices™ Oct 18, 2018 - Oct 19, 2018 Malvern, PA United States
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Oct 22, 2018 - Oct 24, 2018 Malvern, PA United States
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Oct 22, 2018 - Oct 24, 2018 Boston, MA United States
GMPs for OTC & Cosmetic Products - US and Global Requirements Oct 22, 2018 - Oct 23, 2018 Malvern, PA United States
Medical Device Process Validation Training for Professionals Oct 22, 2018 - Oct 24, 2018 Berlin, Germany
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer Oct 22, 2018 - Oct 23, 2018 Malvern, PA United States
Process Validation for Drugs and Biologics Oct 24, 2018 - Oct 25, 2018 Malvern, PA United States
US Cosmetic Manufacturing Regulation - FDA CFR Title 21 Oct 24, 2018 - Oct 26, 2018 Malvern, PA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Oct 25, 2018 - Oct 26, 2018 Berlin, Germany
Product Quality Reviews Oct 25, 2018 - Oct 26, 2018 Boston, MA United States
Formulation Design and Troubleshooting of Dry Dosage Forms Oct 29, 2018 - Oct 30, 2018 Berlin, Germany
Stability Programs for Determining Product Shelf Life Oct 29, 2018 - Oct 30, 2018 Boston, MA United States
Granulation, Tableting and Capsule Technology Oct 31, 2018 - Nov 01, 2018 Berlin, Germany
Preparation of FDA Submissions and Communicating with the FDA Oct 31, 2018 - Nov 01, 2018 Boston, MA United States
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Nov 01, 2018 - Nov 02, 2018 Malvern, PA United States
Lyophilization Technology-Application of Scientific Principles Nov 01, 2018 - Nov 02, 2018 Malvern, PA United States
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Nov 05, 2018 - Nov 06, 2018 Malvern, PA United States
European Union Regulatory Issues - New Product Development Nov 05, 2018 - Nov 06, 2018 Berlin, Germany
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Nov 05, 2018 - Nov 06, 2018 Boston, MA United States
Medical Device Auditing Course: ISO 19011:2011 Framework Nov 05, 2018 - Nov 07, 2018 Malvern, PA United States
Drug Marketing & Advertising of Pharmaceutical & Medical Devices Nov 06, 2018 - Nov 07, 2018 Boston, MA United States
Filing Variations in the European Union™ Nov 07, 2018 - Nov 08, 2018 Berlin, Germany
Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements Nov 07, 2018 - Nov 09, 2018 Boston, MA United States
Medical Device Auditing Course: EN ISO 13485: 2016 Changes Nov 07, 2018 - Nov 09, 2018 Malvern, PA United States
Integration of Risk Management Principles and Activities into the Quality System Nov 12, 2018 - Nov 13, 2018 Los Angeles, CA United States
Cleanroom Microbiology for the Non-Microbiologist Nov 13, 2018 - Nov 14, 2018 Malvern, PA United States
Medical Device Process Validation Training for Professionals Nov 14, 2018 - Nov 15, 2018 Los Angeles, CA United States
Understanding Sterilization Methods for Products and Devices Nov 15, 2018 - Nov 16, 2018 Malvern, PA United States
QbD - Product & Process Optimization using Design of Experiments Nov 26, 2018 - Nov 28, 2018 Berlin, Germany
Clinical Trial Project Management, Phase 1-4 Best Practices Dec 03, 2018 - Dec 05, 2018 Berlin, Germany
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Dec 03, 2018 - Dec 05, 2018 Boston, MA United States
Computer System Validation Dec 06, 2018 - Dec 07, 2018 Los Angeles, CA United States
Writing Effective SOP and Other Process Documents Dec 06, 2018 - Dec 07, 2018 Berlin, Germany
Development & Validation of Bioanalytical Assays for Biologics? Dec 10, 2018 - Dec 11, 2018 Los Angeles, CA United States
Introduction to Effective Medical Writing Dec 10, 2018 - Dec 11, 2018 Boston, MA United States
Technical Writing for Pharma, Biotech and Med Devices Dec 12, 2018 - Dec 14, 2018 Boston, MA United States