SBS - The Best Value in QMS software

Informational From RAPS – EU MDR/IVDR: US Raises ‘Serious Concerns,’ Urges 3-Year Implementation Delay

Elsmar Forum Sponsor

Marcelo

Inactive Registered Visitor
#3
Not sure why, all of the links opened here. Another wya is to copy and paste the title in Google, it will direct you to it.
 
Thread starter Similar threads Forum Replies Date
M Informational From RAPS – UK NB Will Not Apply for EU MDR/IVDR Medical Device and FDA Regulations and Standards News 11
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: Danish Regulators Seek to Help Smaller Companies With EU MDR Compliance Medical Device and FDA Regulations and Standards News 0
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 – Danish Medicines Agency Ramps Up Capacity in Medical Devices 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
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 3
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
F MDR – Article 120 – Transitional provisions EU Medical Device Regulations 2
H MDR Article 13(c) EU Medical Device Regulations 5
Ed Panek Auditor MDR (Presub audit) finding EU Medical Device Regulations 2
M Classification of Instruments under EU MDR EU Medical Device Regulations 1
M Procedure for vigilance system according to new MDR EU Medical Device Regulations 0
M Procedure for clinical evaluation according to new MDR EU Medical Device Regulations 0
R MEDDEV 2.12-1 rev 8 (Vigilance guidelines) still applicable with the MDR implementation? EU Medical Device Regulations 1
S Determining a device category according to the MDR EU Medical Device Regulations 3
A Transactions under MDR Medical Device and FDA Regulations and Standards News 3
H Has anyone undergone MDR FQA review yet? EU Medical Device Regulations 10
S UK MDR + EU MDR Declaration of Conformity UK Medical Device Regulations 0
D Does Risk Management apply to re-labeler (MDR) EU Medical Device Regulations 1
H MDD VS MDR 2002-218 UK Medical Device Regulations 6
Ed Panek MDR Liability Insurance EU Medical Device Regulations 1
S MDD to MDR - Tallow Derivatives Impact EU Medical Device Regulations 1
P Update on NBOG 2014-3 to address MDR/IVDR, or any plan to do that? EU Medical Device Regulations 0
A MDR requirement where unit of use packaging is too small for UDI carrier EU Medical Device Regulations 1
S MDR GSPR Standards EU Medical Device Regulations 1
A MDR - Legacy Device Review Timeframe and Requirements EU Medical Device Regulations 3
J Translation requirements for the statement referred to in ANNEX XIII of MDR EU Medical Device Regulations 0

Similar threads

Top Bottom