Available Courses

Results (137)




Course Title Course Date Location
Clinical Trial Project Management, Phase 1-4 Best Practices Feb 25, 2019 - Feb 27, 2019 Los Angeles, CA United States of America
Preparation of FDA Submissions and Communicating with the FDA Feb 27, 2019 - Feb 28, 2019 Malvern, PA United States of America
Writing Effective SOP and Other Process Documents Feb 28, 2019 - Mar 01, 2019 Los Angeles, CA United States of America
Introduction to Medical Combination Products Mar 04, 2019 - Mar 06, 2019 Boston, MA United States of America
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Mar 06, 2019 - Mar 07, 2019 Los Angeles, CA United States of America
Good Manufacturing Practices Training | GMP Course Mar 06, 2019 - Mar 08, 2019 Malvern, PA United States of America
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Mar 07, 2019 - Mar 08, 2019 Boston, MA United States of America
Lyophilization Technology-Application of Scientific Principles Mar 11, 2019 - Mar 12, 2019 Malvern, PA United States of America
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Mar 13, 2019 - Mar 14, 2019 Malvern, PA United States of America
Pharmaceutical Production Batch Record Review | Training Mar 14, 2019 - Mar 15, 2019 Malvern, PA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Mar 18, 2019 - Mar 19, 2019 Malvern, PA United States of America
GMPs for OTC & Cosmetic Products - US and Global Requirements Mar 18, 2019 - Mar 19, 2019 London, United Kingdom
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Mar 20, 2019 - Mar 21, 2019 El Paso, TX United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Mar 20, 2019 - Mar 22, 2019 Malvern, PA United States of America
Stability Programs for Determining Product Shelf Life Mar 20, 2019 - Mar 21, 2019 Malvern, PA United States of America
US Cosmetic Regulation: FDA CFR Title 21 Training Mar 20, 2019 - Mar 22, 2019 London, United Kingdom
Best Practices for an Effective Cleaning Validation Program Mar 25, 2019 - Mar 26, 2019 Malvern, PA United States of America
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Mar 27, 2019 - Mar 28, 2019 Malvern, PA United States of America
Understanding & Implementing New EU Clinical Trial Regulation & GDPR Mar 27, 2019 - Mar 28, 2019 Malvern, PA United States of America
European Regulatory Procedures - EMA & National Requirements Mar 28, 2019 - Mar 29, 2019 London, United Kingdom
Technical Writing for Pharma, Biotech and Med Devices Apr 01, 2019 - Apr 03, 2019 Malvern, PA United States of America
Biostatistics for Non-Statisticians Apr 03, 2019 - Apr 05, 2019 London, United Kingdom
Clinical Trial Design For Medical Devices™ Apr 03, 2019 - Apr 04, 2019 Boston, MA United States of America
QbD - Product & Process Optimization using Design of Experiments Apr 03, 2019 - Apr 05, 2019 Boston, MA United States of America
Selecting and Managing CROs Apr 04, 2019 - Apr 05, 2019 Malvern, PA United States of America
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Apr 08, 2019 - Apr 10, 2019 Malvern, PA United States of America
Design Control for Medical Device Professionals Apr 08, 2019 - Apr 09, 2019 London, United Kingdom
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Apr 10, 2019 - Apr 12, 2019 London, United Kingdom
Computer System Validation Apr 10, 2019 - Apr 11, 2019 Malvern, PA United States of America
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Apr 10, 2019 - Apr 11, 2019 London, United Kingdom
Specifications for APIs & Pharmaceutical Drug Products Apr 11, 2019 - Apr 12, 2019 Malvern, PA United States of America
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Apr 24, 2019 - Apr 25, 2019 Los Angeles, CA United States of America
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Apr 24, 2019 - Apr 25, 2019 Boston, MA United States of America
The Drug Development Process from Concept to Market Apr 24, 2019 - Apr 26, 2019 London, United Kingdom
European Union Regulatory Issues - New Product Development Apr 29, 2019 - Apr 30, 2019 London, United Kingdom
Technical Writing for Pharma, Biotech and Med Devices Apr 29, 2019 - May 01, 2019 London, United Kingdom
The Drug Development Process from Concept to Market May 01, 2019 - May 03, 2019 Los Angeles, CA United States of America
Writing Effective SOP and Other Process Documents May 02, 2019 - May 03, 2019 London, United Kingdom
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management May 06, 2019 - May 07, 2019 Boston, MA United States of America
Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements May 06, 2019 - May 08, 2019 Malvern, PA United States of America
Integration of Risk Management Principles and Activities into the Quality System May 06, 2019 - May 07, 2019 Malvern, PA United States of America
Introduction to Molecular Biology Techniques May 06, 2019 - May 08, 2019 Malvern, PA United States of America
Product Quality Reviews May 06, 2019 - May 07, 2019 Los Angeles, CA United States of America
Electronic Common Technical Document (eCTD) Submission Training - US vs EU, with Global Insight May 08, 2019 - May 09, 2019 Boston, MA United States of America
Medical Device Process Validation Training for Professionals May 08, 2019 - May 10, 2019 Malvern, PA United States of America
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials May 09, 2019 - May 10, 2019 Malvern, PA United States of America
Preparing the CMC Section for MAAs-IMPDs May 09, 2019 - May 10, 2019 London, United Kingdom
Advanced Blockchain Concepts for the Pharmaceutical and Medical Device Industries May 13, 2019 - May 14, 2019 Malvern, PA United States of America
Design Control for Medical Device Professionals May 13, 2019 - May 14, 2019 Malvern, PA United States of America
QbD - Product & Process Optimization using Design of Experiments May 13, 2019 - May 15, 2019 London, United Kingdom
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars May 15, 2019 - May 17, 2019 London, United Kingdom
Design Validation, Verification, and Risk Analysis for Medical Device Professionals May 15, 2019 - May 16, 2019 Malvern, PA United States of America
Auditing and Qualifying Suppliers and Vendors May 16, 2019 - May 17, 2019 London, United Kingdom
Computer System Validation May 20, 2019 - May 21, 2019 London, United Kingdom
Drug Marketing & Advertising of Pharmaceutical & Medical Devices May 21, 2019 - May 22, 2019 Malvern, PA United States of America
Preparing the CMC Section for NDAs/INDs/CTDs May 22, 2019 - May 23, 2019 Boston, MA United States of America
Process Validation for Drugs and Biologics May 22, 2019 - May 23, 2019 Los Angeles, CA United States of America
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Jun 05, 2019 - Jun 07, 2019 Malvern, PA United States of America
Auditing and Qualifying Suppliers and Vendors Jun 06, 2019 - Jun 07, 2019 Malvern, PA United States of America
European Regulatory Procedures - EMA & National Requirements Jun 10, 2019 - Jun 11, 2019 Malvern, PA United States of America
GMPs for OTC & Cosmetic Products - US and Global Requirements Jun 10, 2019 - Jun 11, 2019 Malvern, PA United States of America
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management Jun 12, 2019 - Jun 13, 2019 Malvern, PA United States of America
Stability Programs for Determining Product Shelf Life Jun 12, 2019 - Jun 13, 2019 Boston, MA United States of America
Biostatistics for Non-Statisticians Jun 17, 2019 - Jun 19, 2019 Boston, MA United States of America
Good Manufacturing Practices Training | GMP Course Jun 17, 2019 - Jun 19, 2019 Los Angeles, CA United States of America
Overview of FDA Regulatory Compliance for Medical Devices Jun 19, 2019 - Jun 20, 2019 Boston, MA United States of America
Advanced Topics in Biostatistics for Non-Statisticians™ Jun 20, 2019 - Jun 21, 2019 Boston, MA United States of America
Basic GMP Training for the QC Laboratory Jun 20, 2019 - Jun 21, 2019 Los Angeles, CA United States of America
Introduction to Statistical Analysis of Laboratory Data Jun 24, 2019 - Jun 25, 2019 Boston, MA United States of America
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Jul 10, 2019 - Jul 11, 2019 Boston, MA United States of America
Lyophilization Technology-Application of Scientific Principles Jul 10, 2019 - Jul 11, 2019 Los Angeles, CA United States of America
Qualifying, Management and Auditing of Contract Manufacturing Organizations Jul 10, 2019 - Jul 11, 2019 Los Angeles, CA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Jul 15, 2019 - Jul 16, 2019 Los Angeles, CA United States of America
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Jul 17, 2019 - Jul 18, 2019 Boston, MA United States of America
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Jul 17, 2019 - Jul 19, 2019 Los Angeles, CA United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Jul 17, 2019 - Jul 19, 2019 Los Angeles, CA United States of America
Introduction to Medical Combination Products Jul 22, 2019 - Jul 24, 2019 Los Angeles, CA United States of America
Technical Writing for Pharma, Biotech and Med Devices Jul 22, 2019 - Jul 24, 2019 Los Angeles, CA United States of America
Best Practices for an Effective Cleaning Validation Program Jul 24, 2019 - Jul 25, 2019 Los Angeles, CA United States of America
Computer System Validation Jul 24, 2019 - Jul 25, 2019 Los Angeles, CA United States of America
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Jul 25, 2019 - Jul 26, 2019 Los Angeles, CA United States of America
Preparation of FDA Submissions and Communicating with the FDA Jul 31, 2019 - Aug 01, 2019 Los Angeles, CA United States of America
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Aug 05, 2019 - Aug 06, 2019 Los Angeles, CA United States of America
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Aug 07, 2019 - Aug 08, 2019 Boston, MA United States of America
Medical Devices: The New MDRs, EU Directives, Guidance, CE Marking and ISO Standard Certifications Aug 07, 2019 - Aug 08, 2019 Los Angeles, CA United States of America
Process Validation for Drugs and Biologics Aug 14, 2019 - Aug 15, 2019 Boston, MA United States of America
Understanding & Implementing New EU Clinical Trial Regulation & GDPR Aug 19, 2019 - Aug 20, 2019 Boston, MA United States of America
Preparing the CMC Section for NDAs/INDs/CTDs Aug 21, 2019 - Aug 22, 2019 Los Angeles, CA United States of America
The Drug Development Process from Concept to Market Aug 21, 2019 - Aug 23, 2019 Boston, MA United States of America
Basic GMP Training for the QC Laboratory Sep 09, 2019 - Sep 10, 2019 Boston, MA United States of America
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Sep 11, 2019 - Sep 12, 2019 Boston, MA United States of America
Stability Programs for Determining Product Shelf Life Sep 11, 2019 - Sep 12, 2019 London, United Kingdom
Good Manufacturing Practices Training | GMP Course Sep 11, 2019 - Sep 13, 2019 Boston, MA United States of America
Design Control for Medical Device Professionals Sep 16, 2019 - Sep 17, 2019 Los Angeles, CA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Sep 16, 2019 - Sep 17, 2019 London, United Kingdom
Overview of FDA Regulatory Compliance for Medical Devices Sep 16, 2019 - Sep 17, 2019 Malvern, PA United States of America
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Sep 18, 2019 - Sep 20, 2019 Boston, MA United States of America
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Sep 18, 2019 - Sep 19, 2019 Los Angeles, CA United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Sep 18, 2019 - Sep 20, 2019 London, United Kingdom
Effective Document Management for Pharma, Biotech & Medical Device Sep 23, 2019 - Sep 24, 2019 Malvern, PA United States of America
GMPs for OTC & Cosmetic Products - US and Global Requirements Sep 23, 2019 - Sep 24, 2019 Boston, MA United States of America
Writing Effective SOP and Other Process Documents Sep 25, 2019 - Sep 26, 2019 Malvern, PA United States of America
Auditing and Qualifying Suppliers and Vendors Oct 03, 2019 - Oct 04, 2019 Boston, MA United States of America
Clinical Trial Design For Medical Devices™ Oct 07, 2019 - Oct 08, 2019 Malvern, PA United States of America
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Oct 16, 2019 - Oct 17, 2019 Boston, MA United States of America
Product Quality Reviews Oct 16, 2019 - Oct 17, 2019 Malvern, PA United States of America
Specifications for APIs & Pharmaceutical Drug Products Oct 16, 2019 - Oct 17, 2019 Los Angeles, CA United States of America
Stability Programs for Determining Product Shelf Life Oct 16, 2019 - Oct 17, 2019 Los Angeles, CA United States of America
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Oct 17, 2019 - Oct 18, 2019 Malvern, PA United States of America
Biostatistics for Non-Statisticians Oct 21, 2019 - Oct 23, 2019 Malvern, PA United States of America
Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements Oct 21, 2019 - Oct 23, 2019 Boston, MA United States of America
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Oct 23, 2019 - Oct 25, 2019 Boston, MA United States of America
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Oct 23, 2019 - Oct 25, 2019 Boston, MA United States of America
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Oct 24, 2019 - Oct 25, 2019 Boston, MA United States of America
Introduction to Statistical Analysis of Laboratory Data Oct 24, 2019 - Oct 25, 2019 Malvern, PA United States of America
Process Validation for Drugs and Biologics Oct 28, 2019 - Oct 29, 2019 Malvern, PA United States of America
Drug Marketing & Advertising of Pharmaceutical & Medical Devices Oct 29, 2019 - Oct 30, 2019 Boston, MA United States of America
Good Manufacturing Practices Training | GMP Course Nov 04, 2019 - Nov 06, 2019 London, United Kingdom
Integration of Risk Management Principles and Activities into the Quality System Nov 04, 2019 - Nov 05, 2019 Los Angeles, CA United States of America
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Nov 06, 2019 - Nov 07, 2019 Malvern, PA United States of America
Medical Device Process Validation Training for Professionals Nov 06, 2019 - Nov 08, 2019 Los Angeles, CA United States of America
Preparation of FDA Submissions and Communicating with the FDA Nov 06, 2019 - Nov 07, 2019 Boston, MA United States of America
Advanced Blockchain Concepts for the Pharmaceutical and Medical Device Industries Nov 07, 2019 - Nov 08, 2019 Los Angeles, CA United States of America
Lyophilization Technology-Application of Scientific Principles Nov 07, 2019 - Nov 08, 2019 Boston, MA United States of America
Best Practices for an Effective Cleaning Validation Program Nov 13, 2019 - Nov 14, 2019 Boston, MA United States of America
Computer System Validation Nov 13, 2019 - Nov 14, 2019 Boston, MA United States of America
Pharmaceutical Production Batch Record Review | Training Nov 14, 2019 - Nov 15, 2019 Boston, MA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Nov 18, 2019 - Nov 19, 2019 Boston, MA United States of America
The Drug Development Process from Concept to Market Nov 18, 2019 - Nov 20, 2019 Malvern, PA United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Nov 20, 2019 - Nov 22, 2019 Boston, MA United States of America
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Dec 02, 2019 - Dec 03, 2019 Malvern, PA United States of America
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Dec 04, 2019 - Dec 06, 2019 Malvern, PA United States of America
Preparing the CMC Section for NDAs/INDs/CTDs Dec 04, 2019 - Dec 05, 2019 Malvern, PA United States of America
Technical Writing for Pharma, Biotech and Med Devices Dec 04, 2019 - Dec 06, 2019 Boston, MA United States of America
Clinical Trial Project Management, Phase 1-4 Best Practices Dec 09, 2019 - Dec 11, 2019 Boston, MA United States of America
Qualifying, Management and Auditing of Contract Manufacturing Organizations Dec 12, 2019 - Dec 13, 2019 Malvern, PA United States of America
Writing Effective SOP and Other Process Documents Dec 12, 2019 - Dec 13, 2019 Boston, MA United States of America