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hum-molgen: events in bioscience and medicine

 
  June, 06 2021
your calendar for events in genetics, biotechnology and medicine
 
              
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- This two day highly interactive course will cover all aspects of radiation sterilization validation, materials selection and processing implementation. This workshop has been designed to help attendee: Radiation Sterilization of Medical Products - Beyond the Basics
- This course is designed to cater for employees of pharmaceutical companies who would like an understanding of the drug development and regulatory approval process. The course starts by considering the: The Drug Development Process from Concept to Market
- The new medical device regulation EU MDR 745/2017 in the European Union has a lot of new requirements. This new upcoming regulation is also stronger connected to the EN ISO 13485:2016. The understandi: Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation
- This 2-day virtual seminar is designed to offer a broad overview of developing and validating a range of assay methodologies for biologics with specific key analysis of cell culture, assay variability: Method Development and Validation for Assays Supporting Testing of Biologics
- This 2 day seminar will go into the specifics of the European Union Medical Device Regulation (EU MDR) and the In Vitro Diagnostic Device Regulation (IVDR), provide case studies and share lessons lear: Fundamentals of EU MDR and IVDR – Level 1
- This Virtual Seminar will provide a great resource to Pharmaceutical, Biotechnology, Diagnostics, Cell Therapy, Drugs, Biologics, OTC, Radio-pharmaceutical, Pharmacies and Medical Device Industries in: Designing and Sustaining New and Existing Product Stability Testing Program
- This FIVE HOUR/DAY, interactive ON-LINE Seminar which provides a conduit to enhance your understanding of the Continued Process Verification, will be reviewed in detail: where does it begin; what is i: Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
- In this two day workshop conference you will learn the requirements and expectations of major health care regulators that are applicable to "virtual" companies. You will learn how to diagnose your com: Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)
- This seminar will help those involved in overcoming these commercial and regulatory obstacles. It will highlight the need for firms to remain current with technological tools and strategy to remain co: FDA's Medical Device Software Regulation Strategy
- This three-day interactive seminar will provide attendees with an understanding of FDA’s veterinary drug approval process. The group size is small, generally between 8 and 20 people, with plenty of op: The Veterinary Drug Approval Process and FDA Regulatory Oversight

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