Company profile

Vigilare

Global Pharmacovigilance and Regulatory Services Provider.

Industry
Biotechnology Research
Employees
174
Headquarters
Ruislip
Founded
2014
Office locations
5

Vigilare company summary

Vigilare is a company in the Biotechnology Research industry, headquartered in Ruislip, founded in 2014. On LinkedIn the company has around 174 employees. The company lists 5 office locations. Its listed specialties include CRO, Regulatory affairs, Regulatory consulting, Pharmacovigilance, Medical Writing.

What technology does Vigilare use?

No technologies detected yet. Warmrank rechecks company websites on a rolling basis.

About Vigilare

We are Vigilare BioPharma, a global Regulatory partner for Pharmaceuticals, Generics, Consumer Healthcare Products and Medical Devices. Founded in 2014, Vigilare Biopharma is a fast-growing, ISO-certified Clinical Research Organization (CRO) focused on the safety assessment and regulatory compliance of pharmaceuticals. Backed by 10+ years of expertise in Life Sciences and MedTech and with a deep understanding of global health authority procedures, including US FDA, EMA, CDSCO, and more, we support the development of safe, effective, and trusted medicinal products and their global market reach. Our goal is to promote the safe and effective use of pharmaceutical products and to ensure that patients receive the trusted quality of care. What We Do? At Vigilare, our priority lies in simplifying challenging regulatory pathways for pharmaceutical and medical device manufacturers. With cross-functional expertise and robust domain knowledge, we bring to the table end-to-end regulatory solutions that span from preclinical to post-market. We are committed to enabling innovative, and compliant product development through our regulatory intelligence-driven specialized Centers of Excellence (CoEs) in: - Pharmacovigilance, - Medical Writing, and - Regulatory Consultation Why Us? We are Vigilare BioPharma. We are proven and certified by global regulatory authorities. Our Certifications include: • ISO 9001:2008 Certified • Backed by EU/US GMP certifications through inspections from leading EU inspectorates • Successfully inspected by global health authorities, including MHRA (UK), USFDA (USA), EMA (Europe), SUKL (Czech Republic), MEB (Netherlands), INFARMED (Portugal), and BfArM (Germany) • Maintained a 100% success rate in regulatory inspections over the last 10 years Facts to Focus • 3,700+ Signal Reports delivered • 52+ Audits & Inspections conducted • 2,600+ Aggregate reports delivered • 9+ Regulatory inspections at client location conducted • 206 K Cases Processed

Specialties

CRORegulatory affairsRegulatory consultingPharmacovigilanceMedical WritingRegulatory ConsultationPublishing ServicesRegulatory Labeling and Technical Writing ServicesRegulatory ComplianceGap Analysis and RemediationQMS Compliance ServicesSubmissions/ RegistrationsMOH Interactions

Where is Vigilare located?

Vigilare lists 5 office locations.

Ruislip, HA46RW, GBHQ
15 Astral Court Ruislip
Bengaluru, Karanataka, IN
Hosur Rd, Krishna Reddy Industrial-Area, Hosapalaya,
Clayton, Victoria, AU
14 Dooga St
Hyderabad, in, IN
San Diego, California, US
8910 University Center Ln

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Frequently asked questions about Vigilare

What does Vigilare do?

We are Vigilare BioPharma, a global Regulatory partner for Pharmaceuticals, Generics, Consumer Healthcare Products and Medical Devices. Founded in 2014, Vigilare Biopharma is a fast-growing, ISO-certified Clinical Research Organization (CRO) focused on the safety assessment and regulatory compliance of pharmaceuticals. Backed by 10+ years of expertise in Life Sciences and MedTech and with a deep understanding of global health authority procedures, including US FDA, EMA, CDSCO, and more, we support the development of safe, effective, and trusted medicinal products and their global market reach. Our goal is to promote the safe and effective use of pharmaceutical products and to ensure that patients receive the trusted quality of care. What We Do? At Vigilare, our priority lies in simplifying challenging regulatory pathways for pharmaceutical and medical device manufacturers. With cross-functional expertise and robust domain knowledge, we bring to the table end-to-end regulatory solutions that span from preclinical to post-market. We are committed to enabling innovative, and compliant product development through our regulatory intelligence-driven specialized Centers of Excellence (CoEs) in: - Pharmacovigilance, - Medical Writing, and - Regulatory Consultation Why Us? We are Vigilare BioPharma. We are proven and certified by global regulatory authorities. Our Certifications include: • ISO 9001:2008 Certified • Backed by EU/US GMP certifications through inspections from leading EU inspectorates • Successfully inspected by global health authorities, including MHRA (UK), USFDA (USA), EMA (Europe), SUKL (Czech Republic), MEB (Netherlands), INFARMED (Portugal), and BfArM (Germany) • Maintained a 100% success rate in regulatory inspections over the last 10 years Facts to Focus • 3,700+ Signal Reports delivered • 52+ Audits & Inspections conducted • 2,600+ Aggregate reports delivered • 9+ Regulatory inspections at client location conducted • 206 K Cases Processed

How many employees does Vigilare have?

Vigilare has around 174 employees on LinkedIn.

Where is Vigilare headquartered?

Vigilare is headquartered in Ruislip.

Where does Vigilare have offices?

Vigilare lists 5 office locations, including Ruislip, HA46RW, GB; Bengaluru, Karanataka, IN; Clayton, Victoria, AU; Hyderabad, in, IN; San Diego, California, US.

When was Vigilare founded?

Vigilare was founded in 2014.

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