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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.

    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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