France Prescription Data

H

hoodyforde

#1
Hi all,

First time poster so apologies for starting with a request for help! I am looking to gather prescriber level data for France, to identify which clinical specialties are prescribing patients to use products similar to our newly introduced therapy. I've had no joy with some of the global market insight players eg IMS Health so I'm wondering if there's anywhere else I can turn to that might be more useful?


Thanks,

D
 
Elsmar Forum Sponsor
Thread starter Similar threads Forum Replies Date
M What is required to run human clinical trials in France EU Medical Device Regulations 9
F EU IVD Registration - Spain / Italy / France / Germany etc EU Medical Device Regulations 7
0 ISO 9001:2008 interpretation not the same per country? (Netherlands and France) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M EU Medical Device Authorized Representative Requirements - France EU Medical Device Regulations 2
I Selling Over the Counter Medical Devices in France EU Medical Device Regulations 3
C New decree in France: Authorization required prior advertising Medical Devices EU Medical Device Regulations 1
E Special Class III Medical Device registration requirements in Germany and France EU Medical Device Regulations 2
C 2012 Registration Tax for Medical Devices and IVD in France EU Medical Device Regulations 0
S IVD Device Registration in France by our local AR EU Medical Device Regulations 5
Gert Sorensen Breast Implant Scandal in France - Industrial Silicone Used in Implants ISO 13485:2016 - Medical Device Quality Management Systems 46
B Country CE Mark Registration Requirements in EU (France and Germany) CE Marking (Conformité Européene) / CB Scheme 7
G Displaying Medical Devices in France & the EU before CE Marking EU Medical Device Regulations 5
Sidney Vianna The last four minutes of Air France flight 447 Federal Aviation Administration (FAA) Standards and Requirements 7
Stijloor The 2009 Tour de France starts on July 4th! Coffee Break and Water Cooler Discussions 3
A France offers loans to Peugeot and Renault World News 0
A Tour de France 2008 Coffee Break and Water Cooler Discussions 24
ScottK 2006 Le Tour de France thread - any cycling enthusiasts among us? Coffee Break and Water Cooler Discussions 37
Marc U.K., Germany, France Competitiveness and Efficiency Slips, WEF Says World News 0
S OTC and Prescription use in EU regulation EU Medical Device Regulations 3
W Direct to customer export of medical device (class I: prescription lenses + frame) US Food and Drug Administration (FDA) 2
M Prescription medical device distribution licenses in the U.S US Food and Drug Administration (FDA) 3
J Restricted device vs. prescription device Medical Device and FDA Regulations and Standards News 1
M Can a PLD Registered in only one state sell prescription drugs to one in another state Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
M Prescription Devices - Who is Responsible / Liable? Other US Medical Device Regulations 9
R Contract Manufacturing - OTC (Over the Counter) vs Prescription Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
M What the FDA considers a Prescription Device - Decisions and Implications Other US Medical Device Regulations 18
N Must electrodes for Rx/prescription stimulators be Rx only? Other US Medical Device Regulations 2
E Documentation for selling Prescription Only Medical Devices Other Medical Device and Orthopedic Related Topics 8
S FDA Approval of Multifunction Device - OTC functions AND Prescription together! Other Medical Device and Orthopedic Related Topics 4
V Prescription Restriction of Medical Devices in EU EU Medical Device Regulations 1
S Switching 510(k) product from Prescription to OTC US Food and Drug Administration (FDA) 2
B New 510k for change to Intended Use - Prescription to OTC 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
S Prescription or non-prescription -Labeling/intended use makes the distinction? Other US Medical Device Regulations 4
A How can I find out if a medical device is prescription only? Other US Medical Device Regulations 4
A FDA Labeling Regulations - 21 CFR part 801.109(c) vs (d): Prescription Labeling Other US Medical Device Regulations 5
M Requirements for Distributor of Prescription Device US Food and Drug Administration (FDA) 6
J Rx Only Statement on Prescription Device Product Label US Food and Drug Administration (FDA) 5
P Generic Contract Manufacturing of Generic Prescription Medications Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 3
P Over The Counter (OTC) vs. POM (Prescription Only Medicine) Other Medical Device Regulations World-Wide 11
S Pharma Code for Prescription Diagnostic Test IVD Other US Medical Device Regulations 1
Q Prescription vs. OTC (Over the Counter) Medical Device in Canada Canada Medical Device Regulations 4
W Class I Medical Device classified as a Prescription Device? Other US Medical Device Regulations 2
J0anne Prescription Only vs. Over The Counter Pharmaceuticals because of State Laws 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
Y Draft FDA Guidance on "Presenting Risk Information in Prescription Drug and Device" US Food and Drug Administration (FDA) 1
M Legal and clinical conditions for defining Prescription-only devices 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
M Prescription Devices and OTC Devices Labeling differences US Food and Drug Administration (FDA) 7
M Can a prescription type material be used as a predicate for an OTC material? Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 1
DuncanGibbons Technical Data Package vs Digital Product Definition APQP and PPAP 0
Z Putting back excluded rows/data points in a control chart Using Minitab Software 0
F General Data Protection Regulation (GDRP) CE Marking (Conformité Européene) / CB Scheme 6

Similar threads

Top Bottom