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Results (94)

Course Title	Course Date	Location
Good Manufacturing Practices (cGMP) Training	No Date Currently Scheduled
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy	No Date Currently Scheduled
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions	Oct 13, 2026 - Oct 15, 2026
Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies	Oct 19, 2026 - Oct 22, 2026
Marketing & Advertising of Pharmaceutical & Medical Devices	Oct 19, 2026 - Oct 21, 2026
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy	Oct 19, 2026 - Oct 22, 2026
Preparing the CMC Section for NDAs/INDs/CTDs	Oct 20, 2026 - Oct 22, 2026
The Drug Development Process from Concept to Market	Oct 26, 2026 - Oct 29, 2026
QbD - Product & Process Optimization using Design of Experiments	Oct 26, 2026 - Oct 29, 2026
Biostatistics for Non-Statisticians	Nov 02, 2026 - Nov 05, 2026
Medical Device Process Validation Training for Professionals	Nov 02, 2026 - Nov 05, 2026
Pharmaceutical Production Batch Record Review	Nov 03, 2026 - Nov 05, 2026
Preparation of FDA Submissions and Communicating with the FDA	Nov 03, 2026 - Nov 05, 2026
Cleaning Validation Best Practices for Drugs, Biologics and Personal Care Products	Nov 09, 2026 - Nov 10, 2026
FDA Inspections - What Regulators Expect and How to Prepare	Nov 09, 2026 - Nov 10, 2026
Laboratory Equipment Validation and Qualification	Nov 12, 2026 - Nov 13, 2026
CMC Regulatory Compliance Strategy for Cell & Gene Therapy Medicines	Nov 16, 2026 - Nov 19, 2026
Specifications for APIs & Pharmaceutical Drug Products	Nov 16, 2026 - Nov 18, 2026
The Drug Development Process from Concept to Market	Nov 16, 2026 - Nov 19, 2026
Computer System Validation	Nov 17, 2026 - Nov 19, 2026
Writing Effective SOP and Other Process Documents	Nov 17, 2026 - Nov 19, 2026
Good Manufacturing Practices (cGMP) Training	Dec 01, 2026 - Dec 04, 2026
OTC Drug and Personal Care Product Regulations and GMPs	Dec 01, 2026 - Dec 04, 2026
Auditing and Qualifying Suppliers and Vendors	Dec 02, 2026 - Dec 04, 2026
Integrating Risk Management into the Pharmaceutical Quality System	Dec 02, 2026 - Dec 03, 2026
Development and Validation of Bioanalytical Assays for Biologics: Quantitation (PK) and Immunogenicity Assays	Dec 07, 2026 - Dec 09, 2026
GMP Training for the QC Laboratory	Dec 07, 2026 - Dec 14, 2026
Technical Writing for Pharma, Biotech and Med Devices	Dec 07, 2026 - Dec 10, 2026
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems	Dec 08, 2026 - Dec 10, 2026
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries	Dec 08, 2026 - Dec 10, 2026
CMC Regulatory Compliance Strategy for Recombinant Proteins, Monoclonal Antibodies, & Biosimilars	Dec 14, 2026 - Dec 17, 2026
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products	Dec 15, 2026 - Dec 17, 2026
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products	Dec 15, 2026 - Dec 17, 2026
Clinical Trial Project Management, Phase 1-4 Best Practices	Jan 11, 2027 - Jan 14, 2027
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management	Jan 18, 2027 - Jan 21, 2027
Introduction to Medical Combination Products	Jan 25, 2027 - Jan 28, 2027
CRO, CDMO and Non-Clinical Vendor Management Fundamentals	Jan 26, 2027 - Jan 28, 2027
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals	Jan 26, 2027 - Jan 28, 2027
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy	Feb 01, 2027 - Feb 04, 2027
Writing Effective SOP and Other Process Documents	Feb 09, 2027 - Feb 11, 2027
Marketing & Advertising of Pharmaceutical & Medical Devices	Feb 16, 2027 - Feb 18, 2027
Good Manufacturing Practices (cGMP) Training	Feb 22, 2027 - Feb 25, 2027
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions	Mar 02, 2027 - Mar 04, 2027
FDA Inspections - What Regulators Expect and How to Prepare	Mar 08, 2027 - Mar 09, 2027
Pharmaceutical Production Batch Record Review	Mar 10, 2027 - Mar 11, 2027
The Drug Development Process from Concept to Market	Mar 15, 2027 - Mar 18, 2027
Technical Writing for Pharma, Biotech and Med Devices	Mar 22, 2027 - Mar 25, 2027
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products	Mar 30, 2027 - Apr 01, 2027
OTC Drug and Personal Care Product Regulations and GMPs	Apr 12, 2027 - Apr 15, 2027
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems	Apr 13, 2027 - Apr 15, 2027
Laboratory Equipment Validation and Qualification	Apr 19, 2027 - Apr 20, 2027
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy	Apr 19, 2027 - Apr 22, 2027
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries	Apr 20, 2027 - Apr 22, 2027
Clinical Trial Project Management, Phase 1-4 Best Practices	Apr 26, 2027 - Apr 29, 2027
Writing Effective SOP and Other Process Documents	May 04, 2027 - May 06, 2027
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management	May 17, 2027 - May 20, 2027
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals	May 18, 2027 - May 20, 2027
Good Manufacturing Practices (cGMP) Training	May 24, 2027 - May 27, 2027
Introduction to Medical Combination Products	May 24, 2027 - May 27, 2027
CRO, CDMO and Non-Clinical Vendor Management Fundamentals	Jun 08, 2027 - Jun 10, 2027
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products	Jun 15, 2027 - Jun 17, 2027
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions	Jun 22, 2027 - Jun 24, 2027
Marketing & Advertising of Pharmaceutical & Medical Devices	Jun 22, 2027 - Jun 24, 2027
Technical Writing for Pharma, Biotech and Med Devices	Jun 28, 2027 - Jul 01, 2027
The Drug Development Process from Concept to Market	Jul 12, 2027 - Jul 15, 2027
FDA Inspections - What Regulators Expect and How to Prepare	Jul 19, 2027 - Jul 20, 2027
Pharmaceutical Production Batch Record Review	Jul 21, 2027 - Jul 22, 2027
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy	Jul 26, 2027 - Jul 29, 2027
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems	Aug 03, 2027 - Aug 05, 2027
OTC Drug and Personal Care Product Regulations and GMPs	Aug 09, 2027 - Aug 12, 2027
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries	Aug 17, 2027 - Aug 19, 2027
Writing Effective SOP and Other Process Documents	Aug 17, 2027 - Aug 19, 2027
Good Manufacturing Practices (cGMP) Training	Aug 30, 2027 - Sep 02, 2027
Cleanroom Fundamentals - Regulation, Science, Design, Practice, Operation & Management	Sep 13, 2027 - Sep 16, 2027
Clinical Trial Project Management, Phase 1-4 Best Practices	Sep 13, 2027 - Sep 16, 2027
Introduction to Medical Combination Products	Sep 13, 2027 - Sep 16, 2027
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products	Sep 21, 2027 - Sep 23, 2027
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals	Sep 21, 2027 - Sep 23, 2027
Marketing & Advertising of Pharmaceutical & Medical Devices	Sep 22, 2027 - Sep 24, 2027
Technical Writing for Pharma, Biotech and Med Devices	Sep 27, 2027 - Sep 30, 2027
CRO, CDMO and Non-Clinical Vendor Management Fundamentals	Oct 12, 2027 - Oct 14, 2027
Laboratory Equipment Validation and Qualification	Oct 12, 2027 - Oct 13, 2027
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy	Oct 25, 2027 - Oct 28, 2027
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions	Oct 26, 2027 - Oct 28, 2027
Writing Effective SOP and Other Process Documents	Nov 08, 2027 - Nov 10, 2027
FDA Inspections - What Regulators Expect and How to Prepare	Nov 15, 2027 - Nov 16, 2027
The Drug Development Process from Concept to Market	Nov 15, 2027 - Nov 18, 2027
Pharmaceutical Production Batch Record Review	Nov 17, 2027 - Nov 18, 2027
Good Manufacturing Practices (cGMP) Training	Nov 29, 2027 - Dec 02, 2027
Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries	Dec 06, 2027 - Dec 08, 2027
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products	Dec 07, 2027 - Dec 09, 2027
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems	Dec 07, 2027 - Dec 09, 2027
OTC Drug and Personal Care Product Regulations and GMPs	Dec 13, 2027 - Dec 16, 2027
Technical Writing for Pharma, Biotech and Med Devices	Dec 13, 2027 - Dec 16, 2027

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Your privacy and trust are important to us. We collect your information only for operational and advisory purposes. We do not and will not sell your private information to a 3rd party. By agreeing to this policy, you are giving us permission to contact you about our services and courses.