RApport Global Strategic Services
RApport is a specialist International regulatory consultancy which was founded in 2003 and offers a range of services to the pharmaceutical, biotechnological and medical device industries. Our focus...load more
RApport Global Strategic Services's Basic Information
Industry
Pharmaceutical Manufacturing
Website
Founded Year
2003
Headcount
11 - 50 ( View All )
Specialties
Regulatory Strategies (Global)Agency Meetings including Scientific AdvicePaediatric Investigational Plans (PIPs)Orphan drugs designationsClinical Trial Applications (CTAs)Project Management (Global)Procedure management – centralised, decentralised, mutual recognition, nationalCommon technical document compilation; Modules 1-5 in ICH regions and beyondPost approval Variations and RenewalsOTCs including switchesLabelling including User Testing
RApport Global Strategic Services's Competitors
Employee Insights
RApport Global Strategic Services's Top Employees
Shaziya Saiyed
Regulatory Affairs Associate AND Pharmacist
Phone Email
Emma Williams
Senior Director Regulatory Affairs
Phone Email
Kelsey Mower
Senior Director Regulatory Affairs
Phone Email
Obaid Khan
Regulatory Affairs Manager
Phone Email
Frequently Asked Questions Regarding RApport Global Strategic Services
How many employees does RApport Global Strategic Services have?
RApport Global Strategic Services has 11 - 50 employees.
What is RApport Global Strategic Services's official website?
RApport Global Strategic Services's official website is http://rapportss.com
What industry does RApport Global Strategic Services belong to?
RApport Global Strategic Services is in the industry ofPharmaceutical Manufacturing
What does RApport Global Strategic Services do?
RApport is a specialist International regulatory consultancy which was founded in 2003 and offers a range of services to the pharmaceutical, biotechnological and medical device industries. Our focus...
What specialty does RApport Global Strategic Services have?
Regulatory Strategies (Global)Agency Meetings including Scientific AdvicePaediatric Investigational Plans (PIPs)Orphan drugs designationsClinical Trial Applications (CTAs)Project Management (Global)Procedure management – centralised, decentralised, mutual recognition, nationalCommon technical document compilation; Modules 1-5 in ICH regions and beyondPost approval Variations and RenewalsOTCs including switchesLabelling including User Testing
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