Informational From RAPS – Danish Medicines Agency Ramps Up Capacity in Medical Devices

Download Free White Paper
Elsmar Forum Sponsor
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
M Informational From RAPS: Danish Regulators Seek to Help Smaller Companies With EU MDR Compliance Medical Device and FDA Regulations and Standards News 0
M RAPS RAC Device - Looking for resources / prep materials & study group Professional Certifications and Degrees 7
cscalise RAPS/Med Dev EU MDR Guidebook - Reviews or Opinions? EU Medical Device Regulations 5
M Informational From RAPS – 27% Will be Compliant? Survey Highlights Lack of Readiness for EU MDR Medical Device and FDA Regulations and Standards News 0
M Informational From RAPS – Novartis Inhaler is First Device to be Certified Under MDR Medical Device and FDA Regulations and Standards News 0
M Informational From RAPS – Operating System Vulnerabilities in Many Medical Devices, Germany’s BfArM and Device Firms Warn Medical Device and FDA Regulations and Standards News 0
M Informational From RAPS – Prep for Brexit: UK Seeks £25M Freight Service to Deliver Medicines, Devices Medical Device and FDA Regulations and Standards News 0
M Informational From RAPS – EU MDR/IVDR: US Raises ‘Serious Concerns,’ Urges 3-Year Implementation Delay Medical Device and FDA Regulations and Standards News 3
M Informational From RAPS – Another Notified Body Bows Out Ahead of EU MDR: ‘Investment Too High’ Medical Device and FDA Regulations and Standards News 2
M Informational From RAPS – UK NB Will Not Apply for EU MDR/IVDR Medical Device and FDA Regulations and Standards News 11
I Should I get IRCA ISO 13485 certification or RAPS certification? Career and Occupation Discussions 3
K RAPS RAC - Resources to prep for the RAC exam that don't cost an arm and a leg Professional Certifications and Degrees 4
S RAPS Regulatory Affairs Certificate Program Training - Internal, External, Online and Distance Learning 1
G RAPS RAC - Regulatory Affairs Certification Help Professional Certifications and Degrees 3
S Mathematics for Regulatory Professionals - RAPS Focus Article Other Medical Device Regulations World-Wide 0
R RAPS Certification Exam Prep Study Group for Spring 2014 Professional Certifications and Degrees 2
S 1st AHWP-RAPS Joint Conference @ KL, Malaysia 2-3 Dec 2013 Other Medical Device Regulations World-Wide 2
S RAPS Article on STED (Summary Technical Documents) Other Medical Device Regulations World-Wide 1
L RAPS RAC EU Certificate: is anyone going to put hands on? Professional Certifications and Degrees 4
Hershal Just for fun raps Coffee Break and Water Cooler Discussions 0
S FDA Enforcements for 2011 - RAPS article on FDA Inspections and Enforcements 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
L RAPS (Regulatory Affairs Professionals Society) books - Are they worth it? Professional Certifications and Degrees 8
S RAC (Regulatory Affairs Certification) from RAPS vs. a University Professional Certifications and Degrees 4
R RAPS Certification Relevant to IT Business Analyst? Professional Certifications and Degrees 4
F What is the duration of the RAPS RAC (EU) Exam? Professional Certifications and Degrees 11
M RAPS RAC - Regulatory Affairs Certification Tips Professional Certifications and Degrees 46
N RAPS Certification and RAPS Testing Professional Certifications and Degrees 1
F RAPS Annual Conference & Exhibition 2010 ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 2
F RAPS Qualification - How Difficult to get are they? Professional Certifications and Degrees 4
M RAPS (Regulatory Affairs Professionals Society) Brazil LinkedIn Network Other Medical Device and Orthopedic Related Topics 0
Z RAPS RAC without Regulatory Experience - Break into the regulatory affairs industry Professional Certifications and Degrees 2
M HACCP - What are the major changes DS 3027:2002 vs. DS 3027:1997 (Danish) Food Safety - ISO 22000, HACCP (21 CFR 120) 1
dgrainger Informational Medicines and Medical Devices Act 2021 UK Medical Device Regulations 0
Aliken Container for the blood bags and medicines EU Medical Device Regulations 2
dgrainger Informational UK - Medicines and Medical Devices Bill 2019-21 UK Medical Device Regulations 0
dgrainger Informational Have your say on the UK's Medicines and Medical Devices Bill Medical Device and FDA Regulations and Standards News 0
J UK Medicines and Medical Devices Bill - 2019 ISO 13485:2016 - Medical Device Quality Management Systems 0
dgrainger Informational UK's new Medicines and Medical Devices Bill Medical Device and FDA Regulations and Standards News 0
M Informational UK – Contingency legislation covering regulation of medicines and medical devices in a no deal scenario – Human Medicines and Medical Devices (Amendm Medical Device and FDA Regulations and Standards News 3
M Informational Medicines and Healthcare Products Regulatory Agency Annual Report and Accounts 2018 to 2019 Medical Device and FDA Regulations and Standards News 0
M Informational UK – Businesses supplying medicines and medical devices – what to expect on day one of a ‘no deal’ scenario Medical Device and FDA Regulations and Standards News 1
M Informational UK – Contingency legislation covering regulation of medicines and medical devices in a no deal scenario Medical Device and FDA Regulations and Standards News 1
M Pharmaceuticals News UK – Further guidance note on the regulation of medicines, medical devices and clinical trials if there’s no Brexit deal Medical Device and FDA Regulations and Standards News 0
somashekar Regulations on Alternative Medicines and Therapy Other Medical Device Regulations World-Wide 1
E External Training - EMEA (European Medicines Agency) Regulations Training - Internal, External, Online and Distance Learning 1
Ajit Basrur Websites - Medicines Regulatory Authorities (global) Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
K Expiry Date for Medicines and Foods Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 3
bio_subbu European Medicines Agency Seeks Comments on Drug/device Consultation Process EU Medical Device Regulations 0
C Drug Registration in European Union - European Medicines Agency (EMEA) Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
T Searching for 6 sigma case studies: medicines, manufacturing Six Sigma 6

Similar threads

Top Bottom