Here you can access all of them with one simple, free registration at the bottom of this page. Or if you already have an Informa Connect account, simply log in below. Have any questions or interested in sponsoring future content? Email andrew.burrows@informa.com.
Medical Device Regulatory Affairs
- Article 117: Preparing Drug Device Combination Product Manufacturers for the EU MDR
- Preparing your organisation for MDSAP: Australia, Canada, Japan, Brazil
- Manufacturing Incident Reports (MIR) under the EU MDR
- MedTech Report 2020: EU MDR and IVDR Compliance
- Comparing EU and FDA approaches to regulating MedTech software and AI
- Assessing new expectations for clinical evaluations and investigations under the EU MDR
- MedTech 2019: State Of The Industry Report
Global Pharma and Biotech Regulatory Affairs
- The use of Real World Evidence and AI within the regulatory landscape
- Building a global regulatory strategy
- Regulatory development opportunities for global harmonisation of eSubmissions
- Global Pharmaceutical Regulatory Affairs State of the Industry Report 2019
- China's changing pharmaceutical regulatory approval
- The Regulatory Environment of Microbiome-Based Therapies in the US and EU
- Regulatory challenges and strategies for oligonucleotide, peptide and mRNA therapeutics
Biocompatability
- Understanding how ISO 10993-17 and ISO 10993-18 connect
- EU MDR: Assessing the impact on biocompatibility testing
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