Available Courses

Results (88)




Course Title Course Date Location
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Jun 02, 2020 - Jun 03, 2020 Virtual (EDT),
Marketing & Advertising of Pharmaceutical & Medical Devices Jun 02, 2020 - Jun 03, 2020 Virtual (EDT),
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Jun 04, 2020 - Jun 05, 2020 Virtual (EDT),
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Jun 08, 2020 - Jun 10, 2020 Virtual (EDT),
Process Validation for Drugs and Biologics Jun 08, 2020 - Jun 09, 2020 Virtual (EDT),
Best Practices for an Effective Cleaning Validation Program Jun 15, 2020 - Jun 16, 2020 Virtual (EDT),
European Regulatory Procedures - EMA & National Requirements Jun 18, 2020 - Jun 19, 2020 Virtual (EDT),
Stability Programs for Determining Product Shelf Life Jun 18, 2020 - Jun 19, 2020 Virtual (CDT),
Preparing the CMC Section for NDAs/INDs/CTDs Jun 24, 2020 - Jun 25, 2020 Virtual (EDT),
The Drug Development Process from Concept to Market Jun 24, 2020 - Jun 26, 2020 Virtual (CDT),
Auditing and Qualifying Suppliers and Vendors Jun 25, 2020 - Jun 26, 2020 Virtual (EDT),
Computer System Validation Jul 13, 2020 - Jul 14, 2020 Virtual (PDT),
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Jul 13, 2020 - Jul 14, 2020 Virtual (EDT),
Medical Devices: The New MDRs, EU Directives, Guidance, CE Marking and ISO Standard Certifications Jul 16, 2020 - Jul 17, 2020 Virtual (EDT),
FDA Inspections - What Regulators Expect and How to Prepare Jul 20, 2020 - Jul 21, 2020 Virtual (EDT),
Writing Effective SOP and Other Process Documents Jul 20, 2020 - Jul 21, 2020 Virtual (PDT),
Biostatistics for Non-Statisticians Jul 21, 2020 - Jul 23, 2020 Virtual (EDT),
Technical Writing for Pharma, Biotech and Med Devices Jul 22, 2020 - Jul 24, 2020 Virtual (PDT),
Qualifying, Management and Auditing of Contract Manufacturing Organizations Jul 27, 2020 - Jul 28, 2020 Virtual (EDT),
Integration of Risk Management Principles and Activities into the Quality System Jul 27, 2020 - Jul 28, 2020 Virtual (PDT),
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Jul 29, 2020 - Jul 31, 2020 Virtual (EDT),
Medical Device Process Validation Training for Professionals Jul 29, 2020 - Jul 31, 2020 Virtual (PDT),
US Cosmetic Regulation: FDA CFR Title 21 Training Aug 03, 2020 - Aug 05, 2020 Virtual (EDT),
Specifications for APIs & Pharmaceutical Drug Products Aug 05, 2020 - Aug 06, 2020 Virtual (EDT),
Design Control for Medical Device Professionals Aug 10, 2020 - Aug 11, 2020 Virtual (CDT),
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Aug 12, 2020 - Aug 13, 2020 Virtual (EDT),
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Aug 17, 2020 - Aug 18, 2020 Virtual (EDT),
Good Manufacturing Practices Training | GMP Course Aug 24, 2020 - Aug 26, 2020 Virtual (PDT),
Technical Writing for Pharma, Biotech and Med Devices Sep 09, 2020 - Sep 11, 2020 Malvern, PA United States of America
Preparing the CMC Section for NDAs/INDs/CTDs Sep 10, 2020 - Sep 11, 2020 Boston, MA United States of America
Effective Document Management for Pharma, Biotech & Medical Device Sep 14, 2020 - Sep 15, 2020 Malvern, PA United States of America
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Sep 14, 2020 - Sep 15, 2020 Boston, MA United States of America
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Sep 14, 2020 - Sep 15, 2020 Los Angeles, CA United States of America
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Sep 14, 2020 - Sep 15, 2020 Boston, MA United States of America
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Sep 15, 2020 - Sep 17, 2020 Boston, MA United States of America
Clinical Trial Project Management, Phase 1-4 Best Practices Sep 16, 2020 - Sep 18, 2020 Malvern, PA United States of America
Preparation of FDA Submissions and Communicating with the FDA Sep 17, 2020 - Sep 18, 2020 Boston, MA United States of America
Lyophilization Technology-Application of Scientific Principles Sep 17, 2020 - Sep 18, 2020 Los Angeles, CA United States of America
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Sep 21, 2020 - Sep 23, 2020 London, United Kingdom
GMPs for OTC & Cosmetic Products - US and Global Requirements Sep 21, 2020 - Sep 22, 2020 Los Angeles, CA United States of America
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Sep 21, 2020 - Sep 22, 2020 Boston, MA United States of America
Auditing and Qualifying Suppliers and Vendors Sep 24, 2020 - Sep 25, 2020 London, United Kingdom
Overview of FDA Regulatory Compliance for Medical Devices Sep 24, 2020 - Sep 25, 2020 Los Angeles, CA United States of America
Product Quality Reviews Oct 01, 2020 - Oct 02, 2020 Malvern, PA United States of America
Stability Programs for Determining Product Shelf Life Oct 01, 2020 - Oct 02, 2020 Boston, MA United States of America
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Oct 05, 2020 - Oct 06, 2020 London, United Kingdom
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Oct 05, 2020 - Oct 07, 2020 Boston, MA United States of America
Medical Device Process Validation Training for Professionals Oct 07, 2020 - Oct 09, 2020 London, United Kingdom
Biostatistics for Non-Statisticians Oct 07, 2020 - Oct 09, 2020 Malvern, PA United States of America
Design Control for Medical Device Professionals Oct 12, 2020 - Oct 13, 2020 London, United Kingdom
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Oct 14, 2020 - Oct 15, 2020 London, United Kingdom
Auditing and Qualifying Suppliers and Vendors Oct 15, 2020 - Oct 16, 2020 Los Angeles, CA United States of America
Selecting and Managing CROs Oct 15, 2020 - Oct 16, 2020 Boston, MA United States of America
Best Practices for an Effective Cleaning Validation Program Oct 15, 2020 - Oct 16, 2020 Los Angeles, CA United States of America
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Oct 19, 2020 - Oct 20, 2020 London, United Kingdom
Pharmaceutical Production Batch Record Review | Training Oct 19, 2020 - Oct 20, 2020 Los Angeles, CA United States of America
Clinical Trial Design For Medical Devices™ Oct 19, 2020 - Oct 20, 2020 Malvern, PA United States of America
Integration of Risk Management Principles and Activities into the Quality System Oct 19, 2020 - Oct 20, 2020 Boston, MA United States of America
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Oct 19, 2020 - Oct 21, 2020 Los Angeles, CA United States of America
Process Validation for Drugs and Biologics Oct 19, 2020 - Oct 20, 2020 Los Angeles, CA United States of America
The Drug Development Process from Concept to Market Oct 20, 2020 - Oct 22, 2020 Boston, MA United States of America
Basic GMP Training for the QC Laboratory Oct 21, 2020 - Oct 22, 2020 Los Angeles, CA United States of America
Medical Device Process Validation Training for Professionals Oct 21, 2020 - Oct 23, 2020 Boston, MA United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Oct 21, 2020 - Oct 23, 2020 Los Angeles, CA United States of America
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Oct 21, 2020 - Oct 23, 2020 Malvern, PA United States of America
European Regulatory Procedures - EMA & National Requirements Oct 22, 2020 - Oct 23, 2020 London, United Kingdom
Qualifying, Management and Auditing of Contract Manufacturing Organizations Oct 22, 2020 - Oct 23, 2020 Los Angeles, CA United States of America
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Oct 22, 2020 - Oct 23, 2020 Malvern, PA United States of America
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Oct 26, 2020 - Oct 28, 2020 London, United Kingdom
The Drug Development Process from Concept to Market Oct 26, 2020 - Oct 28, 2020 London, United Kingdom
Medical Devices: The New MDRs, EU Directives, Guidance, CE Marking and ISO Standard Certifications Oct 26, 2020 - Oct 27, 2020 Boston, MA United States of America
Computer System Validation Nov 09, 2020 - Nov 10, 2020 Boston, MA United States of America
Design Control for Medical Device Professionals Nov 09, 2020 - Nov 10, 2020 Boston, MA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Nov 09, 2020 - Nov 10, 2020 Los Angeles, CA United States of America
Technical Writing for Pharma, Biotech and Med Devices Nov 11, 2020 - Nov 13, 2020 Boston, MA United States of America
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Nov 11, 2020 - Nov 12, 2020 Boston, MA United States of America
Marketing & Advertising of Pharmaceutical & Medical Devices Nov 16, 2020 - Nov 17, 2020 Boston, MA United States of America
Preparing the CMC Section for MAAs-IMPDs Nov 16, 2020 - Nov 17, 2020 London, United Kingdom
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Nov 16, 2020 - Nov 17, 2020 Boston, MA United States of America
Good Manufacturing Practices Training | GMP Course Nov 16, 2020 - Nov 18, 2020 Boston, MA United States of America
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Nov 16, 2020 - Nov 17, 2020 Malvern, PA United States of America
Introduction to Medical Combination Products Nov 18, 2020 - Nov 20, 2020 Boston, MA United States of America
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Nov 19, 2020 - Nov 20, 2020 Malvern, PA United States of America
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Dec 03, 2020 - Dec 04, 2020 Los Angeles, CA United States of America
Good Manufacturing Practices Training | GMP Course Dec 07, 2020 - Dec 09, 2020 London, United Kingdom
The Drug Development Process from Concept to Market Dec 07, 2020 - Dec 09, 2020 Malvern, PA United States of America
Preparing the CMC Section for NDAs/INDs/CTDs Dec 07, 2020 - Dec 08, 2020 Los Angeles, CA United States of America
Understanding & Implementing New EU Clinical Trial Regulation & GDPR Dec 10, 2020 - Dec 11, 2020 Malvern, PA United States of America