FarmavitaR+ International Expert and Service Network
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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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