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        In-House Training

        Bring Our Expert Training In-House

        Looking to train your team without the hassle of travel and adjusting schedules?
        Our in-house training programs are designed to deliver maximum value – on your terms.

        Request an In-House Training

        Why choose an in-house course?

        Learning Objective

        Flexible delivery – onsite or online

        Train your team at the time and place that works best for you. Whether in your offices or virtually, we fit around your schedule.

        Learning Objective

        Cost-efficient solution for entire teams

        Save on multiple delegate fees and travel expenses by training everyone together. A single program equips your whole department with the same knowledge and tools.

        Learning Objective

        Tailored content & interactive workshops

        Get a program that speaks directly to your projects and challenges. We adapt the agenda, case studies, and exercises to your company's real-world needs.

        Some of Our Clients

        Request a Tailored In-House Training

        Fill out this quick form and our team will be in touch to design a program that fits your needs.

        Please describe your training objective or select at least one course. Ideally, both.

        Selected Courses:

          Browse courses by category

          GCP training
          GCP & Data Integrity for Analytical Laboratories – ICH E6 R3 in Practice
          Biometrics in Clinical Trials training course
          Biometrics in Clinical Trials
          clinical investigation evaluation medical device
          Clinical Investigations and Evaluation for Medical Devices
          skates
          Paediatric Drug Development & Clinical Trials
          Orphan Drugs Clinical Trials - Live Online Training
          Orphan Drugs Clinical Trials
          Design Control and Risk Management for Combination Products training
          Design Control and Risk Management For Combination Products
          AI systems in Regulatory and quality for Medical Devices
          AI Systems in Quality & Regulatory Affairs
          Drug-Device Combination Products: Notified Body Opinion Process
          Drug-Device Combination Products: Quality & Regulatory Requirements
          Human Factors for Combination Products
          blood cells
          CMC for Antibody-Drug Conjugates: Strategies for Successful Development and Manufacturing
          CMC and Regulatory Requirements for Inhalation Drug Products
          Process Scale-up and Technology Transfer for Injectables live online training
          Process Scale-up & Tech Transfer for Injectables
          Formulation for Nucleic Acids online training
          CMC/Regulatory Affairs for Nucleic Acids
          CMC Regulatory Compliance for Biologics – A CMC approach to IMPD Walkthrough for Biologics
          Process Development of Solid Dosage Formulations
          Process Development of Solid Dosage Formulations
          Bioequivalence and IVIVC online training
          Bioequivalence and IVIVC
          CMC Statistics
          CMC Module in Regulatory Submissions
          CMC Module in Regulatory Submissions
          CMC Regulatory Requirements for Biosimilars
          CMC Regulatory Requirements for Biosimilars
          CMC Regulatory Compliance for ATMPs
          Aseptic Fill & Finish of Biologics & ATMPs online training course
          Aseptic Fill & Finish of Biologics
          CMC and Regulatory Requirements for Inhalation Drug Products
          Design Control and Risk Management for Combination Products training
          Design Control and Risk Management For Combination Products
          AI systems in Regulatory and quality for Medical Devices
          AI Systems in Quality & Regulatory Affairs
          Drug-Device Combination Products: Notified Body Opinion Process
          Drug-Device Combination Products: Quality & Regulatory Requirements
          Human Factors for Combination Products
          clinical investigation evaluation medical device
          Clinical Investigations and Evaluation for Medical Devices
          Process Scale-up, Validation and Technology Transfer for Medical Devices
          CMO Contracting, Oversight and Value Optimisation
          CMO Contracting, Oversight and Value Optimisation
          Process Scale-up, Technology Transfer and Process Validation course applying QbD principles.
          Process Scale-up, Validation & Technology Transfer
          Lipid Based Formulations
          pharma manufacturing
          Extractables & Leachables Control Strategies
          Process Scale-up and Technology Transfer for Injectables live online training
          Process Scale-up & Tech Transfer for Injectables
          GMP Investigations and Problem Solving Master Class
          GMP Investigations and Problem Solving
          Formulation for Nucleic Acids online training
          CMC/Regulatory Affairs for Nucleic Acids
          CMC Regulatory Compliance for Biologics – A CMC approach to IMPD Walkthrough for Biologics
          Mastering Projects and Regulatory Milestones in Generic Drug Development training
          Mastering Projects and Regulatory Milestones in Generic Drug Development
          Commercial Functions for CDMOs online training
          Commercial Functions for CDMOs
          Process Development of Solid Dosage Formulations
          Process Development of Solid Dosage Formulations
          Bioequivalence and IVIVC online training
          Bioequivalence and IVIVC
          Process Scale-up, Validation and Technology Transfer for Biologics
          dna image
          PK and ADA Assays for Biologics
          data flow
          Statistics for Non-Statisticians
          GMP Lead Auditor
          Advanced Strategies and Future Trends in GMP Auditing
          Aseptic Processing in Manufacture of Sterile Products and ATMPs
          bioassay
          Development and Validation of Bioassays
          oxygen
          VHP/vH2O2 Bio-Decontamination Master Class
          Analytical Method Development and Validation
          Biometrics in Clinical Trials training course
          Biometrics in Clinical Trials
          CMC Statistics
          CMC Module in Regulatory Submissions
          CMC Module in Regulatory Submissions
          CMC Regulatory Requirements for Biosimilars
          CMC Regulatory Requirements for Biosimilars
          flasks in production
          Stability Testing for Biologics
          pharma production
          Equipment Lifecycle Management
          pharma
          Dissolution Testing and Biowaivers
          Advanced Technology Transfer for Pharma & Biotech online training
          Technology Transfer for Pharma & Biotech
          Specifications for Chemical Drug Products
          Specifications for Small Molecule Drug Products
          Strategic Marketing for CDMO Industry online training course
          Strategic Marketing for CDMO Industry
          CMC Regulatory Compliance for ATMPs
          Advancing Real-World Evidence Generation for Causal Inference online training
          Advancing Real-World Evidence Generation for Causal Inference
          Mitigating Immunogenicity Risk
          Mitigating Immunogenicity Risk
          ANNEX 1
          Annex 1 Compliance: Challenges, Solutions and International Impact (EU GMP & PIC/S)
          Quality Requirements for Solids
          Quality Requirements for Solids
          Stability Testing of Biological Drug Products
          Pricing and Market Access of ATMPs online training
          Pricing and Market Access of ATMPs
          statistics
          Statistical Methods Across the Product/ Process Lifecycle
          Development of Solid Generic Formulations online course
          Development of Solid Generic Formulations
          Aseptic Fill & Finish of Biologics & ATMPs online training course
          Aseptic Fill & Finish of Biologics
          Pharma & Biotech Stability Testing
          Pharma & Biotech Stability Testing
          GMP in API Production
          Good Manufacturing Practices in API Production: How to Implement ICHQ7
          skates
          Paediatric Drug Development & Clinical Trials
          Mastery in mRNA Manufacturing: Navigating International Regulations & Best Practices
          Pharmaceutical Cleaning Validation online training course
          Cleaning Validation in Pharma
          quality requirements for biologics
          Quality Requirements for Biologics
          Leverage patient-centric Real-World Evidence (RWE) to accelerate the patient and market access
          Real-World Evidence in Rare Diseases: Accelerating Market Access
          Development of Generic Solid Immediate Release Dosage Forms / Formulation and Analytical Method Development
          This training course integrates the in-vitro dissolution testing, equipment requirements, quality control aspects and using dissolution to obtain biowaivers.
          Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers
          Value Added Medicines training for business development professionals
          Value Added Medicines / Scientific, Regulatory and IP Analysis
          Orphan Drugs Clinical Trials - Live Online Training
          Orphan Drugs Clinical Trials
          Pharmaceutical Quality: QRM, CAPA & Root Cause Analysis
          Process Scale-up, Technology Transfer and Process Validation course applying QbD principles.
          Process Scale-up, Validation & Technology Transfer
          Process Scale-up and Technology Transfer for Injectables live online training
          Process Scale-up & Tech Transfer for Injectables
          Process Scale-up, Validation and Technology Transfer for Biologics
          Aseptic Fill & Finish of Biologics & ATMPs online training course
          Aseptic Fill & Finish of Biologics
          Advanced Industrial Process and Unit Operations Scale-up
          Process Scale-up, Validation and Technology Transfer for Medical Devices
          blood cells
          CMC for Antibody-Drug Conjugates: Strategies for Successful Development and Manufacturing
          CMO Contracting, Oversight and Value Optimisation
          CMO Contracting, Oversight and Value Optimisation
          CMC and Regulatory Requirements for Inhalation Drug Products
          Design Control and Risk Management for Combination Products training
          Design Control and Risk Management For Combination Products
          Process Scale-up, Technology Transfer and Process Validation course applying QbD principles.
          Process Scale-up, Validation & Technology Transfer
          Lipid Based Formulations
          AI systems in Regulatory and quality for Medical Devices
          AI Systems in Quality & Regulatory Affairs
          pharma manufacturing
          Extractables & Leachables Control Strategies
          Process Scale-up and Technology Transfer for Injectables live online training
          Process Scale-up & Tech Transfer for Injectables
          GMP Investigations and Problem Solving Master Class
          GMP Investigations and Problem Solving
          Drug-Device Combination Products: Notified Body Opinion Process
          Formulation for Nucleic Acids online training
          CMC/Regulatory Affairs for Nucleic Acids
          CMC Regulatory Compliance for Biologics – A CMC approach to IMPD Walkthrough for Biologics
          Mastering Projects and Regulatory Milestones in Generic Drug Development training
          Mastering Projects and Regulatory Milestones in Generic Drug Development
          Commercial Functions for CDMOs online training
          Commercial Functions for CDMOs
          Process Development of Solid Dosage Formulations
          Process Development of Solid Dosage Formulations
          Bioequivalence and IVIVC online training
          Bioequivalence and IVIVC
          Process Scale-up, Validation and Technology Transfer for Biologics
          dna image
          PK and ADA Assays for Biologics
          data flow
          Statistics for Non-Statisticians
          GMP Lead Auditor
          Advanced Strategies and Future Trends in GMP Auditing
          Aseptic Processing in Manufacture of Sterile Products and ATMPs
          bioassay
          Development and Validation of Bioassays
          oxygen
          VHP/vH2O2 Bio-Decontamination Master Class
          Analytical Method Development and Validation
          GCP training
          GCP & Data Integrity for Analytical Laboratories – ICH E6 R3 in Practice
          Biometrics in Clinical Trials training course
          Biometrics in Clinical Trials
          CMC Statistics
          Drug-Device Combination Products: Quality & Regulatory Requirements
          CMC Module in Regulatory Submissions
          CMC Module in Regulatory Submissions
          CMC Regulatory Requirements for Biosimilars
          CMC Regulatory Requirements for Biosimilars
          flasks in production
          Stability Testing for Biologics
          pharma production
          Equipment Lifecycle Management
          pharma
          Dissolution Testing and Biowaivers
          Human Factors for Combination Products
          Advanced Technology Transfer for Pharma & Biotech online training
          Technology Transfer for Pharma & Biotech
          Specifications for Chemical Drug Products
          Specifications for Small Molecule Drug Products
          Strategic Marketing for CDMO Industry online training course
          Strategic Marketing for CDMO Industry
          CMC Regulatory Compliance for ATMPs
          Advancing Real-World Evidence Generation for Causal Inference online training
          Advancing Real-World Evidence Generation for Causal Inference
          Mitigating Immunogenicity Risk
          Mitigating Immunogenicity Risk
          ANNEX 1
          Annex 1 Compliance: Challenges, Solutions and International Impact (EU GMP & PIC/S)
          Quality Requirements for Solids
          Quality Requirements for Solids
          Stability Testing of Biological Drug Products
          Pricing and Market Access of ATMPs online training
          Pricing and Market Access of ATMPs
          statistics
          Statistical Methods Across the Product/ Process Lifecycle
          Development of Solid Generic Formulations online course
          Development of Solid Generic Formulations
          Aseptic Fill & Finish of Biologics & ATMPs online training course
          Aseptic Fill & Finish of Biologics
          clinical investigation evaluation medical device
          Clinical Investigations and Evaluation for Medical Devices
          Pharma & Biotech Stability Testing
          Pharma & Biotech Stability Testing
          GMP in API Production
          Good Manufacturing Practices in API Production: How to Implement ICHQ7
          skates
          Paediatric Drug Development & Clinical Trials
          Mastery in mRNA Manufacturing: Navigating International Regulations & Best Practices
          Pharmaceutical Cleaning Validation online training course
          Cleaning Validation in Pharma
          quality requirements for biologics
          Quality Requirements for Biologics
          Leverage patient-centric Real-World Evidence (RWE) to accelerate the patient and market access
          Real-World Evidence in Rare Diseases: Accelerating Market Access
          Development of Generic Solid Immediate Release Dosage Forms / Formulation and Analytical Method Development
          This training course integrates the in-vitro dissolution testing, equipment requirements, quality control aspects and using dissolution to obtain biowaivers.
          Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers
          Value Added Medicines training for business development professionals
          Value Added Medicines / Scientific, Regulatory and IP Analysis
          Advanced Industrial Process and Unit Operations Scale-up
          Orphan Drugs Clinical Trials - Live Online Training
          Orphan Drugs Clinical Trials
          Pharmaceutical Quality: QRM, CAPA & Root Cause Analysis
          Process Scale-up, Validation and Technology Transfer for Medical Devices
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