Webinars and in-house training
Webinars, seminars and in-house training courses
At GxPedia GmbH, we offer a variety of training formats to keep your team up to date with the latest developments and best practices in the pharmaceutical and medical device industries:
Discover our attractive webinar and in-house training packages that are tailored specifically to the needs of your team.
We offer both fixed training packages and the option of customizing the content and duration of training courses to meet your requirements. Our goal is to provide you and your team with the necessary knowledge and skills to operate successfully in the pharmaceutical industry and meet regulatory requirements.
Our training courses
Our training courses are designed to provide you and your team with the knowledge and skills you need to operate successfully in the pharmaceutical industry and meet regulatory requirements.
Webinars
Our interactive online webinars offer a convenient way to learn about specific topics in the pharmaceutical industry, GxP, medical devices and quality management. You can take part in our webinars live, ask questions and benefit from expert knowledge without leaving your office.
In-house training courses
On request, we can organize tailor-made in-house training courses directly at your company. We focus on the specific needs and requirements of your team and ensure that the training content is practical and applicable.
Offer webinars and in-house training
Standard package consisting of the specified modules 1 – 4: 2.100,00 €**
Individual composition*: 600,00 € per module**
Standard package “Medical devices”
(4 Module a 90 min)
- Module 1: Legal basis MDR
- Module 2: Certification
- Module 3: Clinical evaluation and clinical trial
- Module 4: Medical device classification workshop
Standard package “Validation”
(4 Module a 90 min)
- Module 1: Legal basis for validation
- Module 2: Smart process validation strategies
- Module 3: Cleaning validation
- Module 4: Validation workshop
Standard package “GMP basics”
(4 Module a 90 min)
- Module 1: German GMP regulations
- Module 2: EU and US GMP regulations
- Module 3: Documentation (Chapter 4 EU GMP Guideline)
- Module 4: Quality control (Chapter 6 EU GMP Guideline)
Standard package “Pharmaceutical production”
(4 Module a 90 min)
- Module 1: Pharmaceutical production (Chapter 5 EU-GMP Guide)
- Module 2: Personnel (Chapter 2 EU-GMP Guide)
- Module 3: Premises (Chapter 3 EU GMP Guide)
- Module 4: Equipment (Chapter 3 EU-GMP Guide)
Standard package “Deviations”
(4 Module a 90 min)
- Module 1: Regulatory basics
- Module 2: Deviation management process
- Module 3: Classification systems
- Module 4: Deviations workshop
Standard package “GMP audits”
(4 Module a 90 min)
- Module 1: Overview of GMP audits
- Module 2: Smart audit management
- Module 3: Classification of audit findings
- Modul 4: Workshop Auditsituationen
Standard package “Method verification and method validation”
(4 Module a 90 min)
- Module 1: Regulatory overview
- Module 2: Organization
- Module 3: Changes
- Module 4: Method transfers and method transfer plans
Standard package “Biologics”
(4 Module a 90 min)
- Module 1: Regulatory basics
- Module 2: Quality requirements
- Module 3: Manufacturing requirements
- Module 4: Process validation requirements
Standard package “Solids”
(4 Module a 90 min)
- Module 1: Regulatory requirements
- Module 2: Quality requirements
- Modul 3: Kontinuierliche Fertigung
- Module 4: Case study coating solutions
*from over 120 different modules in the fields of Medical Devices and Combination Products, Pharmaceutical Packaging, Validation & Qualification, GMP, Deviations, Topica, Workshop, Audits, QC, Change Controls, GxP, Regulatory, Biologics, Solids, mRNA (please contact us)
**Prices are valid for an online webinar. In-house training available starting from 4 modules plus additional fees. Arrival and overnight stay
Secure your consultation appointment
Ask for an individual consultation to find out more about our wide range of training options!
