Regulatory and Pharmacovigilance Consulting
REGULATOP is a leading pharmaceutical manufacturing consultancy, specializing in regulatory affairs and pharmacovigilance. Located in Rho, Milan, REGULATOP offers comprehensive support to pharmaceutical companies, ensuring full assistance and time-effective results in navigating the complex regulatory landscape. With a focus on quality and compliance, REGULATOP stands as a reliable partner for companies seeking expert guidance. REGULATOP is committed to supporting pharmaceutical companies with specialized services. From dossier preparation to regulatory support, the company ensures adherence to the highest standards. REGULATOP's primary address is Via F. Baracca 10, Rho, Milan 20017, IT.
REGULATOP excels in providing a range of services, including medical writing, CTD/eCTD preparation, and pharmacovigilance support. Their expertise extends to medical devices and includes EU & Italian regulatory support, along with local QPPV services. REGULATOP's thorough approach and commitment to excellence make them an invaluable asset to any pharmaceutical company aiming for regulatory success.
REGULATOP's dedication to quality and compliance positions them as a key player in the pharmaceutical industry. The company continues to expand its capabilities to meet the evolving needs of its clients, ensuring they remain at the forefront of regulatory and pharmacovigilance developments. We invite the manager of REGULATOP to create a customized and exclusive company showcase and product listing on our platform.
Compare REGULATOP with 3 companies in Pharmaceutical-Manufacturing
| Comparison Field |
REGULATOPMain Company |
MeetView Profile |
PaspigioniView Profile |
Evidenze ItalyView Profile |
|---|---|---|---|---|
|
Founded Year
|
— | 2009 | 2015 | 2001 |
|
Company Size
|
— | 51-200 | 11-50 | 501-1,000 |
|
City
|
Rho, Milan | London, London | London, England | Milano, MI |
|
Country
|
United Kingdom | United Kingdom | Italy | |
|
Skills & Keywords
Comparing with main company
|
12 Total Skills
Pharmaceutical Manufacturing
Regulatory Affairs
Pharmacovigilance
Medical Writing
Quality Compliance
CTD/eCTD
QPPV Services
Quality Compliance/PV Auditing
EU & Italian Regulatory Support; local QPPV
Medical Devices
Pharmacovigilance support / EU QPPV
Dossier preparation & maintenance
|
15 Total
2 Common
13 Unique
Match
17%
Common Skills:
Pharmacovigilance
Regulatory Affairs
Unique Skills:
Account Management
Client Services
Clinical Operations
Data & Biometrics
Digital
Healthcare Advertising
+7
|
6 Total
6 Unique
Unique Skills:
Data Management & Statistics
Feasibility & Site Selection
Monitoring & Site Management
Quality Support & Auditing
Regulatory Support
Translations & Logistics
|
7 Total
7 Unique
Unique Skills:
Clinical Research
Data Management & Statistics
Monitoring
No-profit & IDS studies
Project Management
Regulatory
+1
|
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