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alina_subtirica

0 0 Reviews €75 EUR/hr

Skills:

Regulatory submissions Meetings with Authorities Scientific advice Orphan Drug Biological, biosimilar National pharmacovigilance Risk Managment Plan Adverse Events Processing National market access support P&R support for generics P&R support for innovative medicines Rx to OTC switch MA transfer Translations Literature Monitoring Variation Type I Variation Type II Grouped Variations OTC Pharmaceutial Medical Device Generic Pharmaceuticals Innovative Pharmaceuticals Food Supplements Readability User Testing

Business Name: Alina Subtirica

Vilpharm

0 0 Reviews €100 EUR/hr

Skills:

Dossier compilation Regulatory submissions Meetings with Authorities National market access support Pharmaco-economic study P&R support for generics P&R support for innovative medicines Business Analysis Business Plans Project Management Rx to OTC switch MA transfer Translations Communications to Healthcare Practicioners Business Development Variation Type I Variation Type II Grouped Variations OTC Pharmaceutial Medical Device Generic Pharmaceuticals Innovative Pharmaceuticals Food Supplements European Union Statistics

Business Name: dsokac

ivanabd@yahoo.com

0 0 Reviews €60 EUR/hr

Skills:

Dossier compilation Dossier lifecycle management Regulatory submissions Meetings with Authorities Orphan Drug Hybrid Product National pharmacovigilance National market access support Pharmaco-economic study P&R support for generics P&R support for innovative medicines MA transfer Translations Communications to Healthcare Practicioners Business Development Literature Monitoring Variation Type I Variation Type II Grouped Variations OTC Pharmaceutial Medical Device Generic Pharmaceuticals Innovative Pharmaceuticals Food Supplements Rest of Europe (non EU)

Business Name: RAMACO

koen.laenen@pharmavize.com

0 0 Reviews €85 EUR/hr

Skills:

Dossier compilation eCTD, NeeS publishing Dossier lifecycle management Regulatory submissions Meetings with Authorities Scientific advice Orphan Drug Vaccines Hybrid Product Risk Managment Plan P&R support for generics Project Management MA transfer Translations Social Media Communications GxP Audit Periodic Safety Update Reports

koen.laenen@pharmavize.com

0 0 Reviews €125 EUR/hr

Skills:

Process development Formulation development Stability study Dossier compilation eCTD, NeeS publishing Dossier lifecycle management Regulatory submissions Meetings with Authorities Scientific advice Orphan Drug Biological, biosimilar Vaccines Blood derivatives, stem cells Hybrid Product Risk Managment Plan P&R support for generics Project Management Rx to OTC switch MA transfer Translations GxP Training GxP Audit Periodic Safety Update Reports

rss

0 0 Reviews €80 EUR/hr

Skills:

Dossier compilation Dossier lifecycle management Regulatory submissions National pharmacovigilance International pharmacovigilance Validated PV database Adverse Events Processing P&R support for generics Project Management MA transfer Literature Monitoring Variation Type I Variation Type II Grouped Variations OTC Pharmaceutial Medical Device Generic Pharmaceuticals North America South America European Union Rest of Europe (non EU)Readability User Testing

Business Name: rss

Lozda

0 0 Reviews €120 EUR/hr

Skills:

Dossier compilation eCTD, NeeS publishing Dossier lifecycle management Regulatory submissions Meetings with Authorities Scientific advice National pharmacovigilance International pharmacovigilance Adverse Events Processing National market access support International market access support Pharmaco-economic study P&R support for generics P&R support for innovative medicines Rx to OTC switch MA transfer Translations Literature Monitoring Variation Type I Variation Type II Grouped Variations OTC Pharmaceutial Cosmetic Products Food Supplements Borderline Product

Business Name: FMS BALTIC

s_dhallu

0 0 Reviews €30 EUR/hr

Skills:

Process development Formulation development Stability study BE study Dossier compilation eCTD, NeeS publishing Dossier lifecycle management Regulatory submissions Scientific advice Orphan Drug P&R support for generics Licensing GxP Audit Variation Type I Variation Type II Grouped Variations Super-grouped Variations Generic Pharmaceuticals North America South America European Union Rest of Europe (non EU)Africa Middle East Asia & Australia

tntuan

0 0 Reviews €120 EUR/hr

Skills:

Preclinical study Drug delivery design eCTD, NeeS publishing Dossier lifecycle management Regulatory submissions Orphan Drug Biological, biosimilar International pharmacovigilance International market access support Pharmaco-economic study P&R support for generics P&R support for innovative medicines Rx to OTC switch OTC Pharmaceutial Medical Device

Business Name: IBC Asia

zmauko

0 0 Reviews €100 EUR/hr

Skills:

Process development Formulation development eCTD, NeeS publishing Regulatory submissions Meetings with Authorities Scientific advice International pharmacovigilance Validated PV database International market access support P&R support for generics P&R support for innovative medicines MA transfer Social Media Communications GxP Audit Literature Monitoring Periodic Safety Update Reports European Union Rest of Europe (non EU)Readability User Testing ISO Audit

Business Name: Farmavita Regulanet d.o.o.

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