GMP for Mid-Level Management in the Pharmaceutical Industry
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GMP for Mid-Level Management in the Pharmaceutical Industry

This training provides an overview of the key aspects of quality control for middle management.

  • Based on 963 participants

GMP & GDP training for pharma & biotech

  • Language:
    Dutch flag English flag
  • 3 days in total

€ 1956.00 ex. VAT

Registration ends in 85 days.

Register now!

This training contains:
  • Accreditation for openbaar apothekers (KNMP), 19.5 accreditation points
  • Accreditation for ziekenhuisapothekers (NVZA), 19.5 accreditation points
  • Lunch
  • Course dinner
  • Digital copy of materials
  • Training certificate

    • What you will learn

    Implementing GMP from theory to practice, including Quality Culture

    Effectively deal with the unique position of mid-level management in the pharmaceutical industry

    Identify the importance and essence of GMP, through a solid understanding of the rules and regulations

    Training Dates

    Dates Language Price Register
    3/18/25 to 3/20/25 English spoken language (primary) € 1956.00 Register
    5/13/25 to 5/15/25 Dutch spoken language (primary) € 1956.00 Register
    9/16/25 to 9/18/25 Dutch spoken language (primary) € 1956.00 Register
    11/25/25 to 11/27/25 Dutch spoken language (primary) € 1956.00 Register

    Description

    The Training

    This three-day course provides an overview of the key aspects of quality management for middle management.

    This well-established course offers an overview of the most important aspects of quality control. Knowledge and understanding at the middle management level play an indispensable role in this. This group is often heavily involved in setting up, improving, and applying quality systems. The training covers the essential elements of a quality system and supporting activities such as validation, qualification, and change control. This year, the course content has been updated to reflect the latest developments in GMP concerning the changes in European guidelines.

    Please note! The March edition will be conducted in English unless there are no English-speaking participants in attendance.

    Target Audience

    This training is frequently attended by QA Officers & Managers, QPs, QC Managers & Analysts, and Production Managers or Supervisors. It is suitable for those at the bachelor's or master's degree level.

    This training is also suitable for openbaar apothekers and ziekenhuisapothekers, who will receive professional accreditation points.

    Results

    • GMP is easier to interpret and translate into practice
    • Insight into 'gaps' within the organization
    • Awareness of the importance of GMP in daily operations

    Contents

    • Laws and regulations
    • Quality Culture
    • Quality Systems
    • Documentation and Data Integrity
    • Validation
    • Raw materials and APIs
    • Pharmaceutical production (including packaging)
    • Quality Control
    • Outsourcing activities
    • Complaints and recalls
    • Storage and Distribution
    • Experiences of the Dutch Health and Youth Care Inspectorate (IGJ)
    • GMP in your own practice

    Lecturers

    Karen Zimmermann avatar

    Karen Zimmermann

    Trainer

    Pharmaceutical trainer, consultant, and coach with over 20 years of expertise in GMP (Good Manufacturing Practice) a...

    Jolanda Tijmes avatar

    Jolanda Tijmes

    Trainer

    Experienced senior consultant with extensive expertise in quality management within the pharmaceutical industry, wit...

    Program

    Practical Information

    Accreditation:
    Difficulty / Level:
    Beginner level and Intermediate level
    Group discounts:
    • 2 participants - 5%
    • 3 participants - 10%
    • 4 participants - 15%
    • 4 participants - 20%
    • 6+ participants - 25%

    Group discounts are only applicable when multiple participants register for the same course at the same time.

    Language (upcoming edition):
    • en flag English spoken language (primary)
    • Some lectures/lessons may be in the secondary language. The primary language remains the dominant spoken/written language during the training.
    Learning form:
    Classroom
    Times:
    Starts at 09:30 and ends at 17:30
    Notes to the course dinner:

    At the end of day 2, you will be offered a course dinner.

    Tags

    Change Control GMP GDP EudraLex Volume IV Medicines Act Deviations Quality Assurance QC Calibration Validation Qualification CSV Quality Culture Packaging Sampling Batch Review Manufacturing Distribution CCS OOS Qualified Person Human Error Batch Record Quality Awareness Complaints Personnel Licenses PIC/S ICH Risk Management Training Facility Equipment Cleaning Validation Documentation Annex 11 Computerized Systems Data Integrity GDocP Critical Parameters Sampling Outsourcing Risk Ranking Recall Returns IGJ Self Inspection

    Reviews (269)

    4 out of 5 stars

    Based on 269 reviews

    Review data

    5 star reviews

    35%

    4 star reviews

    58%

    3 star reviews

    6%

    2 star reviews

    1%

    1 star reviews

    0%

    Reviews prior to 2017 were paper-based and are not included below.

    4 out of 5 stars

    Strong points (and why):

    How to approach improving quality culture in my team and lock gmp in everything we do

    Review:

    Grip on the entirety of gmp. When IGJ is invited and you allow questions over lunch and to connect with the inspector, then do not sit with three PCS personnel around the inspectors at the table, preventing most training participants from being able to make contact.

    Maarten - Sr Facility Manager

    4 out of 5 stars

    Strong points (and why):

    Diepgang

    Jeffrey Buntsma - supervisor engineering

    4 out of 5 stars

    Strong points (and why):

    Er zijn veel onderwerpen aan bod gekomen en je werd tijdens de training gestimuleerd om dit te vertalen naar de eigen werkvloer.

    Nikki Wildhagen - QA Compliance Specialist

    4 out of 5 stars

    Strong points (and why):

    Genoeg afwisseling

    Review:

    Vaker beweegmomenten. Ga zo door!

    Melissa Scholte - QA officer

    5 out of 5 stars

    Strong points (and why):

    Alle onderwerpen werden behandeld

    Joke Beukers - QC analist

    4 out of 5 stars

    Strong points (and why):

    De interactie

    Jasper - Automation engineer

    5 out of 5 stars

    Strong points (and why):

    De kansen om vragen te stellen

    Matthias Groeneveld - Quality assistent manager

    5 out of 5 stars

    Strong points (and why):

    Juridische wetten vertalen naar praktijk. Afwisseling presentaties en workshops. Presentaties gasten.

    Yvonne Hilkes - Kwaliteitsmedewerker

    4 out of 5 stars

    Strong points (and why):

    Afwisseling van onderwerpen en veel ruimte voor vragen.

    Rikst - Analist

    4 out of 5 stars

    Strong points (and why):

    Duidelijke uitleg, trainers van goede kwaliteit

    Review:

    Eudralex boekje met wat label er tussen zodat je goed de hoofdstukken en annexen kan opzoeken. Niet zo’n lange workshop aan het eind.

    Amber - Junior GxP Consultant

    5 out of 5 stars

    Strong points (and why):

    Interactiviteit en de diepgang van de stof.

    Review:

    Super gedaan en bedankt voor de info! Krijgen we het SLA voorbeeld van de spreker?

    Karlijn - Hoofd productie

    5 out of 5 stars

    Strong points (and why):

    Goede informatie, genoeg workshops tussendoor

    Audrey - Productie specialist

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    Registration ends in 85 days.

    Register now!

    Difficulty:
    Beginner level Intermediate level
    This training contains:
  • Accreditation for openbaar apothekers (KNMP), 19.5 accreditation points
  • Accreditation for ziekenhuisapothekers (NVZA), 19.5 accreditation points
  • Lunch
  • Course dinner
  • Digital copy of materials
  • Training certificate
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