Available Courses

Results (101)




Course Title Course Date Location
Technical Writing for Pharma, Biotech and Med Devices Sep 27, 2017 - Sep 29, 2017 Berlin, Germany
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Oct 02, 2017 - Oct 03, 2017 Malvern, PA United States
Good Manufacturing Practices Training | GMP Course Oct 02, 2017 - Oct 04, 2017 Los Angeles, CA United States
Regulated Medical Marijuana Business - Concept to Product Sale Oct 04, 2017 - Oct 05, 2017 Malvern, PA United States
Introduction to Molecular Biology Techniques Oct 11, 2017 - Oct 13, 2017 Malvern, PA United States
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries Oct 12, 2017 - Oct 13, 2017 Malvern, PA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Oct 12, 2017 - Oct 13, 2017 Berlin, Germany
Advanced Topics in Biostatistics for Non-Statisticians™ Oct 16, 2017 - Oct 17, 2017 Malvern, PA United States
Computer System Validation Oct 16, 2017 - Oct 17, 2017 Boston, MA United States
Integration of Risk Management Principles and Activities into the Quality System Oct 16, 2017 - Oct 17, 2017 Berlin, Germany
Preparation of FDA Submissions and Communicating with the FDA Oct 16, 2017 - Oct 17, 2017 Malvern, PA United States
Effective Document Management for Pharma, Biotech & Medical Device Oct 17, 2017 - Oct 18, 2017 Malvern, PA United States
Biostatistics for Non-Statisticians Oct 18, 2017 - Oct 20, 2017 Malvern, PA United States
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Oct 18, 2017 - Oct 20, 2017 Malvern, PA United States
Medical Device Validation Training for Professionals Oct 18, 2017 - Oct 20, 2017 Berlin, Germany
Selecting and Managing CROs Oct 19, 2017 - Oct 20, 2017 Malvern, PA United States
Stability Programs for Determining Product Shelf Life Oct 23, 2017 - Oct 24, 2017 Malvern, PA United States
The Drug Development Process from Concept to Market Oct 23, 2017 - Oct 25, 2017 Boston, MA United States
The Electronic Common Technical Document (eCTD): Strategies & Tools to Build a Successful Submission Oct 23, 2017 - Oct 24, 2017 Los Angeles, CA United States
Water Purification Systems for Regulated Industries Oct 23, 2017 - Oct 24, 2017 Berlin, Germany
Writing Effective SOP and Other Process Documents Oct 23, 2017 - Oct 24, 2017 Malvern, PA United States
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Oct 24, 2017 - Oct 26, 2017 Berlin, Germany
Heating, Ventilation & A/C in a Regulated Environment Oct 25, 2017 - Oct 27, 2017 Berlin, Germany
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Oct 25, 2017 - Oct 27, 2017 Malvern, PA United States
US Cosmetic Manufacturing Regulation - FDA CFR Title 21 Oct 25, 2017 - Oct 27, 2017 Los Angeles, CA United States
Auditing and Qualifying Suppliers and Vendors Oct 30, 2017 - Oct 31, 2017 Berlin, Germany
Formulation Design and Troubleshooting of Dry Dosage Forms Oct 30, 2017 - Oct 31, 2017 Berlin, Germany
Medical Device Auditing Course: ISO 19011:2011 Framework Oct 30, 2017 - Nov 01, 2017 Malvern, PA United States
Granulation, Tableting and Capsule Technology Nov 01, 2017 - Nov 02, 2017 Berlin, Germany
Medical Device Auditing Course: EN ISO 13485:2016 Changes Nov 01, 2017 - Nov 03, 2017 Malvern, PA United States
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products Nov 02, 2017 - Nov 03, 2017 Malvern, PA United States
Lyophilization Technology-Application of Scientific Principles Nov 02, 2017 - Nov 03, 2017 Malvern, PA United States
Auditing and Qualifying Suppliers and Vendors Nov 06, 2017 - Nov 07, 2017 Malvern, PA United States
FDA Inspections - What Regulators Expect and How to Prepare Nov 06, 2017 - Nov 07, 2017 Berlin, Germany
GMPs for OTC & Cosmetic Products - US and Global Requirements Nov 06, 2017 - Nov 07, 2017 Los Angeles, CA United States
Integration of Risk Management Principles and Activities into the Quality System Nov 06, 2017 - Nov 07, 2017 Los Angeles, CA United States
Introduction to Effective Medical Writing Nov 06, 2017 - Nov 07, 2017 Malvern, PA United States
Overview of FDA Regulatory Compliance for Medical Devices Nov 06, 2017 - Nov 07, 2017 Malvern, PA United States
Preparing the CMC Section for NDAs/INDs/CTDs Nov 06, 2017 - Nov 07, 2017 Los Angeles, CA United States
Clinical Trial Design For Medical Devices™ Nov 08, 2017 - Nov 09, 2017 Malvern, PA United States
Global Personal Care Market & Regulatory Overview Nov 08, 2017 - Nov 10, 2017 Los Angeles, CA United States
Medical Device Validation Training for Professionals Nov 08, 2017 - Nov 10, 2017 Los Angeles, CA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Nov 08, 2017 - Nov 10, 2017 Berlin, Germany
Technical Writing for Pharma, Biotech and Med Devices Nov 08, 2017 - Nov 10, 2017 Malvern, PA United States
Cleanroom Microbiology for the Non-Microbiologist Nov 13, 2017 - Nov 14, 2017 Malvern, PA United States
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Nov 13, 2017 - Nov 14, 2017 Malvern, PA United States
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Nov 13, 2017 - Nov 15, 2017 Berlin, Germany
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Nov 13, 2017 - Nov 14, 2017 Los Angeles, CA United States
Good Clinical Practices (GCP) & Risk Based Monitoring - Understanding and Implementing Current Global Requirements Nov 15, 2017 - Nov 17, 2017 Malvern, PA United States
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Nov 15, 2017 - Nov 16, 2017 Los Angeles, CA United States
Understanding Sterilization Methods for Products and Devices Nov 15, 2017 - Nov 16, 2017 Malvern, PA United States
Preparing the CMC Section for MAAs-IMPDs Nov 16, 2017 - Nov 17, 2017 Berlin, Germany
QbD - Product & Process Optimization using Design of Experiments Nov 22, 2017 - Nov 24, 2017 Berlin, Germany
Design Control for Medical Device Professionals Nov 28, 2017 - Nov 29, 2017 Malvern, PA United States
Best Practices for an Effective Cleaning Validation Program Nov 29, 2017 - Nov 30, 2017 Berlin, Germany
Design Validation, Verification, and Risk Analysis for Medical Device Professionals Nov 30, 2017 - Dec 01, 2017 Malvern, PA United States
Product Quality Reviews Nov 30, 2017 - Dec 01, 2017 Malvern, PA United States
European Regulatory Procedures - EMA & National Requirements Dec 04, 2017 - Dec 05, 2017 Berlin, Germany
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies Dec 04, 2017 - Dec 06, 2017 Malvern, PA United States
Good Manufacturing Practices Training | GMP Course Dec 04, 2017 - Dec 06, 2017 Malvern, PA United States
Water Purification Systems for Regulated Industries Dec 04, 2017 - Dec 05, 2017 Malvern, PA United States
Heating, Ventilation & A/C in a Regulated Environment Dec 06, 2017 - Dec 08, 2017 Malvern, PA United States
Computer System Validation Dec 07, 2017 - Dec 08, 2017 Los Angeles, CA United States
Development & Validation of Bioanalytical Assays for Biologics Dec 07, 2017 - Dec 08, 2017 Los Angeles, CA United States
Effective Document Management for Pharma, Biotech & Medical Device Dec 11, 2017 - Dec 12, 2017 Berlin, Germany
Understanding & Implementing New EU Clinical Trial Regulation Dec 11, 2017 - Dec 12, 2017 Malvern, PA United States
The Drug Development Process from Concept to Market Dec 13, 2017 - Dec 15, 2017 Malvern, PA United States
Writing Effective SOP and Other Process Documents Dec 13, 2017 - Dec 14, 2017 Berlin, Germany
Biostatistics for Non-Statisticians Jan 22, 2018 - Jan 24, 2018 Los Angeles, CA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Jan 22, 2018 - Jan 23, 2018 Los Angeles, CA United States
The Drug Development Process from Concept to Market Jan 22, 2018 - Jan 24, 2018 Los Angeles, CA United States
Introduction to Medical Combination Products Jan 24, 2018 - Jan 26, 2018 Los Angeles, CA United States
Understanding & Implementing New EU Clinical Trial Regulation Jan 25, 2018 - Jan 26, 2018 Los Angeles, CA United States
Best Practices for an Effective Cleaning Validation Program Jan 29, 2018 - Jan 30, 2018 Los Angeles, CA United States
Clinical Trial Project Management, Phase 1-4 Best Practices Jan 29, 2018 - Jan 31, 2018 Los Angeles, CA United States
European Union Regulatory Issues - New Product Development Jan 29, 2018 - Jan 30, 2018 Berlin, Germany
Filing Variations in the European Union™ Jan 31, 2018 - Feb 01, 2018 Berlin, Germany
Effective Document Management for Pharma, Biotech & Medical Device Feb 01, 2018 - Feb 02, 2018 Los Angeles, CA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Feb 05, 2018 - Feb 06, 2018 Los Angeles, CA United States
Selecting and Managing CROs Feb 05, 2018 - Feb 06, 2018 Los Angeles, CA United States
Drug Marketing & Advertising of Pharmaceutical & Medical Devices Feb 07, 2018 - Feb 08, 2018 Malvern, PA United States
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Feb 07, 2018 - Feb 08, 2018 Los Angeles, CA United States
Writing Effective SOP and Other Process Documents Feb 07, 2018 - Feb 08, 2018 Los Angeles, CA United States
CMC Regulatory Compliance for Biopharmaceuticals & Biosimilars Feb 12, 2018 - Feb 14, 2018 Los Angeles, CA United States
ADME, PK/TK & Drug Metabolism in Drug Discovery and Development Feb 21, 2018 - Feb 23, 2018 Los Angeles, CA United States
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Feb 21, 2018 - Feb 23, 2018 Los Angeles, CA United States
Development & Validation of Bioanalytical Assays for Biologics Feb 26, 2018 - Feb 27, 2018 Berlin, Germany
Auditing and Qualifying Suppliers and Vendors Mar 01, 2018 - Mar 07, 2018 Boston, MA United States
Product Quality Reviews Mar 01, 2018 - Mar 02, 2018 Los Angeles, CA United States
Lyophilization Technology-Application of Scientific Principles Mar 01, 2018 - Mar 02, 2018 Los Angeles, CA United States
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products Mar 05, 2018 - Mar 06, 2018 Boston, MA United States
FDA Inspections - What Regulators Expect and How to Prepare Mar 05, 2018 - Mar 06, 2018 Los Angeles, CA United States
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer Mar 05, 2018 - Mar 06, 2018 Boston, MA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Mar 07, 2018 - Mar 09, 2018 Los Angeles, CA United States
Process Validation for Drugs and Biologics Mar 07, 2018 - Mar 08, 2018 Boston, MA United States
Project Management for Medical Device Product Development Mar 08, 2018 - Mar 09, 2018 Los Angeles, CA United States
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions Mar 12, 2018 - Mar 13, 2018 Berlin, Germany
Introduction to Medical Combination Products Mar 14, 2018 - Mar 16, 2018 Berlin, Germany
QbD - Product & Process Optimization using Design of Experiments Mar 19, 2018 - Mar 21, 2018 Boston, MA United States
Biostatistics for Non-Statisticians Mar 26, 2018 - Mar 28, 2018 Berlin, Germany
The Drug Development Process from Concept to Market Mar 26, 2018 - Mar 28, 2018 Berlin, Germany