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Wed, 09 Jan 2019 2pm
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certifiednutra
0
0 Reviews
Skills:
Formulation development
Food Supplements
North America
European Union
Middle East
Business Name:
Certified Nutraceuticals
AWe
0
0 Reviews
€100 EUR/hr
Skills:
Dossier compilation
Regulatory submissions
Meetings with Authorities
National market access support
MA transfer
Translations
GxP Training
GxP Audit
Validation Protocol Development
QA Policy Development
Qualified Person for BR
Variation Type I
Variation Type II
Grouped Variations
Medical Device
Generic Pharmaceuticals
European Union
ISO Training
ISO Audit
Business Name:
Aleksander Wegner
anava
0
0 Reviews
€90 EUR/hr
Skills:
eCTD, NeeS publishing
Regulatory submissions
Medical Device
Generic Pharmaceuticals
South America
European Union
Rest of Europe (non EU)
Russia and CIS
Africa
Middle East
Asia & Australia
Augur
0
0 Reviews
€4 EUR/hr
Skills:
National pharmacovigilance
International pharmacovigilance
Validated PV database
Risk Managment Plan
Adverse Events Processing
International market access support
Pharmaco-economic study
Literature Monitoring
Periodic Safety Update Reports
European Union
Rest of Europe (non EU)
Azhar Faridi
0
0 Reviews
€30 EUR/hr
Skills:
Process development
Toxicology
Preclinical study
Phase I clinical study
Phase II clinical study
Regulatory submissions
Vaccines
Risk Managment Plan
Adverse Events Processing
National market access support
International market access support
Pharmaco-economic study
Social Media Communications
Communications to Healthcare Practicioners
Business Development
QA Policy Development
Literature Monitoring
Variation Type I
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
Food Supplements
North America
European Union
Asia & Australia
Basiak11
0
0 Reviews
Skills:
Project Management
GxP Audit
European Union
LacertaBio
0
0 Reviews
€200 EUR/hr
Skills:
Biological, biosimilar
Business Analysis
Business Plans
Business Development
Licensing
Innovative Pharmaceuticals
North America
European Union
Business Name:
LacertaBio
Con-ORC
0
0 Reviews
€50 EUR/hr
Skills:
BE study
Phase I clinical study
Phase II clinical study
Phase III clinical study
Regulatory submissions
Orphan Drug
Biological, biosimilar
National pharmacovigilance
Adverse Events Processing
Human Resources
Project Management
Recruitment
Communications to Healthcare Practicioners
GxP Audit
Literature Monitoring
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
European Union
Business Name:
Con-ORC
Deepti
0
0 Reviews
€30 EUR/hr
Skills:
Process development
Adverse Events Processing
Literature Monitoring
Periodic Safety Update Reports
European Union
Protocols and SOPs Development
Business Name:
Pharmacovigilance
bherenyi
0
0 Reviews
€100 EUR/hr
Skills:
Dossier compilation
Translations
GxP Training
GxP Audit
Variation Type I
Variation Type II
Grouped Variations
OTC Pharmaceutial
Generic Pharmaceuticals
Innovative Pharmaceuticals
Food Supplements
European Union
Rest of Europe (non EU)
Fortunaa
0
0 Reviews
€30 EUR/hr
Skills:
Dossier compilation
Regulatory submissions
Meetings with Authorities
Scientific advice
Orphan Drug
Biological, biosimilar
Vaccines
Blood derivatives, stem cells
Hybrid Product
National pharmacovigilance
International pharmacovigilance
Risk Managment Plan
National market access support
Accounting
Business Analysis
Business Plans
Human Resources
Legal Research
Project Management
Public Relations
MA transfer
Translations
Social Media Communications
Communications to Healthcare Practicioners
Business Development
Licensing
Communications to Payers
Periodic Safety Update Reports
Variation Type I
Variation Type II
Grouped Variations
Super-grouped Variations
OTC Pharmaceutial
Veterinary Pharmaceutical
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
Cosmetic Products
Food Supplements
North America
South America
European Union
Rest of Europe (non EU)
Russia and CIS
Africa
Middle East
Asia & Australia
Borderline Product
Communications to Patients
Business Name:
Fusion
jukkar
0
0 Reviews
€145 EUR/hr
Skills:
Process development
Formulation development
Stability study
BE study
Toxicology
Preclinical study
Phase I clinical study
Phase III clinical study
Regulatory submissions
Orphan Drug
Biological, biosimilar
Communications to Healthcare Practicioners
Business Development
GxP Training
GxP Audit
Validation Protocol Development
QA Policy Development
OTC Pharmaceutial
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
Cosmetic Products
North America
European Union
Asia & Australia
billev
0
0 Reviews
€80 EUR/hr
Skills:
Dossier lifecycle management
Regulatory submissions
International pharmacovigilance
Risk Managment Plan
National market access support
GxP Training
European Union
Protocols and SOPs Development
Business Name:
Billev farmacija vzhod d.o.o.
margaj
0
0 Reviews
€10 EUR/hr
Skills:
Phase II clinical study
Phase III clinical study
Dossier compilation
Regulatory submissions
National pharmacovigilance
National market access support
Communications to Healthcare Practicioners
OTC Pharmaceutial
Generic Pharmaceuticals
Innovative Pharmaceuticals
European Union
Russia and CIS
Business Name:
Margarita
marpas
0
0 Reviews
€100 EUR/hr
Skills:
Regulatory submissions
Meetings with Authorities
Vaccines
National pharmacovigilance
International pharmacovigilance
Validated PV database
Adverse Events Processing
National market access support
Project Management
MA transfer
Translations
Literature Monitoring
Periodic Safety Update Reports
OTC Pharmaceutial
Medical Device
Generic Pharmaceuticals
Cosmetic Products
European Union
Readability User Testing
Business Name:
-
martina
0
0 Reviews
€90 EUR/hr
Skills:
Formulation development
Stability study
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Meetings with Authorities
Scientific advice
Rx to OTC switch
MA transfer
GxP Training
GxP Audit
QA Policy Development
Medical Device
Cosmetic Products
Food Supplements
European Union
Protocols and SOPs Development
ISO Training
ISO Audit
Business Name:
FamavitaR+
mihnic
0
0 Reviews
€115 EUR/hr
Skills:
Dossier compilation
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Orphan Drug
Biological, biosimilar
Vaccines
National market access support
MA transfer
Translations
Variation Type I
Variation Type II
Grouped Variations
Super-grouped Variations
OTC Pharmaceutial
Generic Pharmaceuticals
Innovative Pharmaceuticals
South America
European Union
Rest of Europe (non EU)
Russia and CIS
Africa
Middle East
Readability User Testing
Protocols and SOPs Development
mchica
0
0 Reviews
€50 EUR/hr
Skills:
Toxicology
Preclinical study
Scientific advice
Translations
Literature Monitoring
European Union
Rest of Europe (non EU)
mirshahroz
0
0 Reviews
€30 EUR/hr
Skills:
Dossier compilation
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Scientific advice
Biological, biosimilar
International pharmacovigilance
Risk Managment Plan
MA transfer
Periodic Safety Update Reports
Variation Type I
Variation Type II
Grouped Variations
Medical Device
Generic Pharmaceuticals
Food Supplements
European Union
Rest of Europe (non EU)
Russia and CIS
Africa
Middle East
Asia & Australia
Borderline Product
Protocols and SOPs Development
ISO Audit
Business Name:
Medwisdom Lifesciences Private Limited
NiconMedical
0
0 Reviews
€55 EUR/hr
Skills:
Dossier compilation
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Meetings with Authorities
Biological, biosimilar
MA transfer
Translations
Social Media Communications
Communications to Healthcare Practicioners
Literature Monitoring
Variation Type I
Variation Type II
Grouped Variations
Super-grouped Variations
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
Cosmetic Products
European Union
Communications to Patients
Protocols and SOPs Development
Business Name:
Nicon Medical
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