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certifiednutra
0
0 Reviews
Skills:
Formulation development
Food Supplements
North America
European Union
Middle East
Business Name:
Certified Nutraceuticals
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
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
US FDA consultant
0
0 Reviews
€125 EUR/hr
Skills:
Phase I clinical study
Phase II clinical study
Phase III clinical study
Dossier compilation
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Meetings with Authorities
International market access support
Project Management
Translations
Social Media Communications
Business Development
QA Policy Development
Periodic Safety Update Reports
OTC Pharmaceutial
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
Cosmetic Products
Food Supplements
North America
Rest of Europe (non EU)
Russia and CIS
Protocols and SOPs Development
Business Name:
Pattern of USA
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
Fortunaaag
0
0 Reviews
€50 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
Validated PV database
Risk Managment Plan
Adverse Events Processing
National market access support
International market access support
Pharmaco-economic study
Business Analysis
Business Plans
Project Management
Public Relations
Rx to OTC switch
MA transfer
Translations
Social Media Communications
Communications to Healthcare Practicioners
Business Development
Licensing
Communications to Payers
Literature Monitoring
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:
Fortuna Gorani BI
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
leticiac3
0
0 Reviews
€70 EUR/hr
Skills:
Regulatory submissions
Meetings with Authorities
Legal Research
Public Relations
Cosmetic Products
Food Supplements
North America
South America
Business Name:
R Leticia Cuevas
pravee.bits@gmail.com
0
0 Reviews
€20 EUR/hr
Skills:
Formulation development
Dossier compilation
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Scientific advice
Orphan Drug
OTC Pharmaceutial
Generic Pharmaceuticals
North America
European Union
Rest of Europe (non EU)
Russia and CIS
Africa
Middle East
Asia & Australia
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
rajbai
0
0 Reviews
€15 EUR/hr
Skills:
Formulation development
Stability study
BE study
Dossier compilation
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Adverse Events Processing
QA Policy Development
Variation Type I
Variation Type II
North America
Africa
Asia & Australia
Ravis
0
0 Reviews
€20 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
Hybrid Product
Validated PV database
Rx to OTC switch
MA transfer
Business Development
Licensing
Periodic Safety Update Reports
Variation Type I
Variation Type II
Grouped Variations
Super-grouped Variations
OTC Pharmaceutial
Generic Pharmaceuticals
Innovative Pharmaceuticals
North America
European Union
Rest of Europe (non EU)
Russia and CIS
Africa
Middle East
Asia & Australia
Readability User Testing
Business Name:
RS
rihabgama
0
0 Reviews
€45 EUR/hr
Skills:
Preclinical study
Phase I clinical study
Phase II clinical study
Phase III clinical study
Regulatory submissions
Scientific advice
Vaccines
Blood derivatives, stem cells
National pharmacovigilance
International pharmacovigilance
Adverse Events Processing
National market access support
International market access support
Pharmaco-economic study
Project Management
Literature Monitoring
Periodic Safety Update Reports
Medical Device
Innovative Pharmaceuticals
North America
Africa
Middle East
Protocols and SOPs Development
Business Name:
Rihab Gamaoun
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
sindhura
0
0 Reviews
€25 EUR/hr
Skills:
Dossier compilation
eCTD, NeeS publishing
Dossier lifecycle management
Regulatory submissions
Variation Type I
Variation Type II
Generic Pharmaceuticals
Cosmetic Products
North America
European Union
Rest of Europe (non EU)
Africa
Middle East
sripadaraja
0
0 Reviews
€65 EUR/hr
Skills:
Phase I clinical study
Phase II clinical study
Phase III clinical study
Orphan Drug
Biological, biosimilar
National pharmacovigilance
International pharmacovigilance
Validated PV database
Risk Managment Plan
Adverse Events Processing
Project Management
Literature Monitoring
Periodic Safety Update Reports
Medical Device
Generic Pharmaceuticals
North America
European Union
Rest of Europe (non EU)
Middle East
Asia & Australia
Protocols and SOPs Development
Business Name:
Joish Pharma and Life sciences consulting
Asepticsme
0
0 Reviews
€150 EUR/hr
Skills:
Process development
Formulation development
Drug delivery design
Phase III clinical study
Orphan Drug
Biological, biosimilar
Vaccines
International market access support
Business Plans
Rx to OTC switch
MA transfer
GxP Training
GxP Audit
QA Policy Development
Qualified Person for BR
OTC Pharmaceutial
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
North America
South America
Rest of Europe (non EU)
Russia and CIS
Asia & Australia
Protocols and SOPs Development
Business Name:
asepticsme
Roestuff
0
0 Reviews
€330 EUR/hr
Skills:
Process development
Meetings with Authorities
Orphan Drug
Biological, biosimilar
Vaccines
National pharmacovigilance
International pharmacovigilance
Validated PV database
Risk Managment Plan
Adverse Events Processing
Business Plans
Project Management
Communications to Healthcare Practicioners
QA Policy Development
Literature Monitoring
Periodic Safety Update Reports
OTC Pharmaceutial
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
North America
South America
European Union
Communications to Patients
Protocols and SOPs Development
Business Name:
M2D Global Life Sciences
zdrmau
0
0 Reviews
€50 EUR/hr
Skills:
Orphan Drug
Biological, biosimilar
Vaccines
Blood derivatives, stem cells
Hybrid Product
Social Media Communications
Business Development
Licensing
Communications to Payers
GxP Audit
Validation Protocol Development
QA Policy Development
OTC Pharmaceutial
Veterinary Pharmaceutical
Medical Device
Generic Pharmaceuticals
Innovative Pharmaceuticals
Cosmetic Products
Food Supplements
North America
European Union
Rest of Europe (non EU)
Russia and CIS
Middle East
Borderline Product
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