Welcome to
PharmaVigilance Limited

We understand exactly how critical it is to maintain the quality of services to maintain compliance with regulatory requirements

Read More

Welcome to
Pharma Vigilance Limited

We understand exactly how critical it is to maintain the quality of services to maintain compliance with regulatory requirements

Read More

About Us

PharmaVigilance Limited is a knowledge process outsourcing company which provides a range of services in the area of Pharmacovigilance (PV) and Regulatory Affairs. We ensure a cost-effective support to our clients with high standards of quality. The company was established in 2013 and is based in Slough, United Kingdom. We offer a range of pharmacovigilance services to pharmaceutical companies of all sizes in the UK. Our clients are highly satisfied with our quality of services, thus providing us with repeat business and outsourcing many PV related activities, considering our competitive charges for all activities undertaken by us.

Our Mission

“Always delivering high standards of Quality and Excellence is our mission.”

PharmaVigilance team works on the trail of “Quality and Integrity” that help us in understanding the requirements of our clients. Our rooted values with exceptional functioning practices ensure the excellent client service on our all appointments. We are a growing organisation and we believe that our outstanding results today, will lay the standards for the establishment in the future.

Our Vision

“Our vision is to be a trendsetter in the consulting industry with our innovative and consistent approach assuring high quality standards and client satisfaction.”

PharmaVigilance is a knowledge process outsourcing company that emphasises on the core ethics and standards to meet our client needs and satisfaction. We believe in deep association and collaboration of our working groups which help us to innovate in a way that others cannot. Our determination, hard work and passion constitute our core values which comprise the whole structure of our organisation.

Our Services

PharmaVigilance is a service provider for various aspects of PV, Medical Writing, Regulatory Affairs and Publishing Services. We provide our expert services throughout the development, approval and post-approval stages of a product's lifecycle to small, mid and large sized pharmaceutical and biotechnology companies worldwide. To find out more about our services please click below on the specific services you are interested in:

Pharmacovigilance & Drug safety Services

PharmaVigilance team develops and implements customised strategies for PV and Drug safety services. PV and all drug safety issues are relevant to every person whose life is touched in any way by medical interventions. …

Regulatory Affairs Services

PharmaVigilance encompasses the reputable Regulatory Affairs team, which comprises of experienced professionals, who provide simplified assistance in the drug approval process for various geographical areas, especially for Europe and the United States …

Publishing
Services

We have in-house facility to publish and submit the electronic and paper-based regulatory submissions to the Regulatory Authorities. We provide full submission lifecycle support of the product through our elite publishing software system …

Other Medical writing Services

PharmaVigilance serves the needs of various pharmaceutical companies as per regulatory requirements. We provide regulatory and medical writing services throughout the lifecycle of the product, from preclinical development to marketing authorisation and product …

PV Medical writing Services

PharmaVigilance team is well experienced in writing different types of PV documents and can provide a comprehensive solution to a client for aggregate reporting. We can support you with the writing of various documents such as …

Regulatory Affairs Services

PharmaVigilance encompasses the reputable Regulatory Affairs team, which comprises of experienced professionals, who provide simplified assistance in the drug approval process for various geographical areas, especially …

Auditing Services

Due to the stringent regulations and increasing demands from Regulatory Authorities, the pharmaceutical companies must ensure that a robust PV system. We can help you to achieve this to high standards with our following services …

Publishing Services

We have in-house facility to publish and submit the electronic and paper-based regulatory submissions to the Regulatory Authorities. We provide full submission lifecycle support of the product through our elite publishing software system …

Other Medical writing Services

PharmaVigilance serves the needs of various pharmaceutical companies as per regulatory requirements. We provide regulatory and medical writing services throughout the lifecycle of the product, from preclinical development …

Training and Workshop Services

According to the regulations, all personnel involved in the performance of PV activities within an organisation must receive initial and continued training. We provide bespoke training covering different aspects of PV and so can customise the content …

Testimonials

Dr Zoe Farrington

European Medical Affairs Director for a Multinational Biotech Company, United Kingdom.

“I had the pleasure of working with Upasana over the course of a nine-month period, during which time she provided consultancy services to our start-up biotech. In addition to providing regulatory and pharmacovigilance services, which involved writing the risk management plan and the DDPS for the company’s product, and writing pre-marketing authorisation SOPs to support the pharmacovigilance system, Upasana guided us with her professional advice at every step until we were granted marketing authorisation for our product in the EU. She also performed the role of QPPV, a role that she fulfilled more than adequately, consistently providing sound advice and proving to be someone of reliability who was always willing to help. In addition to her consummate professionalism, her humour, generosity, dedication to the tasks in question and willingness to help were appreciated by everyone. I would recommend her without reservation.”

Dr Judit Széll, MD

Ex-QPPV for a Global Pharmaceutical company, based in Budapest, Hungary.

"The Company has been providing us their impeccable services in the area of documentation writing and auditing for a long time now. We have found them to be very helpful and knowledgeable. They have been excellent writers and auditors, explaining requirements, and steering us expertly and helpfully. They have demonstrated a lot of flexibility to work around our requirements and timelines, offering to undertake extra tasks when there was scarcity of time and resource at our end. The team is always very accommodating, pro-active, helpful and hard-working. We appreciate their invaluable support and advice, customising their services in the best possible way to suit our requirements."

Ildikó Hajdu-Németh, MD

Senior Executive for a Global Pharmaceutical company, based in Budapest, Hungary.

“The expertise of the Company has been a significant value-add to our Pharmacovigilance System. The consultants provide up-to- date knowledge of the changing regulations of European Guidelines on Good Pharmacovigilance Practices (GVP). The Company has been providing various PV services through the years which include PV System set-up, maintenance, GVP gap analysis, GVP inspection readiness, as well as authoring a wide range of safety documents such as PBRERs, PSURs and DSURs. We can count on PharmaVigilance to keep their commitments and deliver high standards of quality work, within agreed timelines and budget. We appreciate their loyalty, diligence, flexibility and quality!"

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Get in Touch

Contact Info

Address

PharmaVigilance Limited
Slough, United Kingdom
Ph: +44 (0) 7557797291
uprabhakar@pharma-vigilance.co.uk
info@pharma-vigilance.co.uk

Contact Info

PharmaVigilance
United Kingdom
P: +44 (0) 7557797291
uprabhakar@pharma-vigilance.co.uk
info@pharma-vigilance.co.uk