Our focus and strength is in providing professional and reliable support to our clients, often in the short timeframe they need it.
As we have personally confronted and effectively managed the typical challenges facing Industry, we are primed to respond and act quickly.
We use deep industry insight gained from personal hands-on experience as well as by leveraging the cumulative exposure of our partner and consultant network, to be able to deliver specific solutions and/or resourcing models.
It is our amazing team and network that makes us who we are. Our core leadership and consultant partner team alone has in excess of 140 years of collective experience working in all aspects of the regulatory and pharmacovigilance sectors of the Pharmaceutical Industry. Our individual and joint success is down to making no compromises when it comes to quality of what we deliver, the responsiveness of our engagement, the flexibility of our individuals in the entire organisation and the support reliability that affords our clients peace of mind.
We have working knowledge and systems experience in 8 of the top 10 global pharma companies and have collectively worked at most levels within the industry, time served in large pharma, speciality pharma, branded and generics, large and small molecules.
Our team of freelancers are positioned in most of the major geographies and supplement Regulink’s wide and varied skill set that we know is necessary to work in the complex environment of Regulatory Affairs and Pharmacovigilance.
We feel this allows us to rapidly understand our client’s needs to faciliate rapid onboarding and project kick off.
Through our diverse team, Regulink is able to act as a round-the-clock service provider, in synergy with the client. This enables our partners to continue to operate as normal and take advantage of the market and region-specific expertise and intelligence from our team in all of its project strategies.
We realise there is a need for ad hoc rapid resource, often for short term assignments, because of the very dynamic regulatory environment the Pharmaceutical sector works in. We know first hand that this can be hard for larger providers to achieve. Regulink is set up perfectly to deliver this to its clients. This is what sets us apart.
Regulink welcomes the opportunity to discuss the unique regulatory and pharmacovigilance consulting services that it provides and how it might benefit your organisation
Regulink is a small but growing team of professionals in Regulatory Affairs and Pharamcovigilance. By working with Regulink, you will be operating as a consultant on client projects, supporting them and adding value. You will be able to provide your experience and expertise, as well as develop and expand your skill set from working with like-minded individuals in Regulink project teams.
Regulink was founded by long time colleagues and friends, Stuart and Sunil. Their close working relationship became the modus operandi of the Company. We work with and treat our clients and consultants as valuable partners.
The media and industry attention to off-payroll working (IR35) and the reforms for the private sector that are due to take place in 2021, will be no surprise to many contractors out there. It represents what could be a big change to the way many contractors have to work, whether they like it or not. Regulink has a partnership with QDOS an IR35 insurance specialist to ensure that all of our contractors are fully checked and insured with regards to IR35. This means we work directly with our clients to meet industry IR35 requirements.
Please contact us about your requirements or to discuss our services or solutions in more detail.
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Whether it be a special regulatory project, intelligence, strategy or support with the essential life cycle management aspects, Regulink provides solutions that have delivered successful and cost-effective outcomes time after time. We are proud of the range and quality of services that we can provide, evidenced by the long term working partnerships we have established with our varied client list. Although not an exhaustive list, the main areas of our expertise and services are shown below:
Regulink provides pharmacovigilance services tailored to support your business needs. Our UK-based in-house QPPV has extensive experience from working as an EU and UK QPPV, with demonstrated leadership and management of large PV projects and teams of PV officers. We understand that all projects and clients are unique, so as with Regulatory Affairs, we offer a fully flexible service and work closely throughout to ensure your requirements are always met. The main expertise and services provided are shown below:
Regulink was established by industry veterans, Stuart Reed and Sunil Singh, in 2014, following lengthy independent careers within industry and consultancy organisations. With recent changes to the consulting landscape, Regulink has rapidly grown to take on core partners with highly valuable and niche experience, as well as expanding its consulting partner network to be able to cater for its clients of all sizes. Regulink now offers consulting and other services in UK, Europe, US and Australia, supported by local expertise, and continues to grow, whilst always providing the flexible and scalable services that industry needs.
Read our expert’s thoughts on industry news and regulatory topics.
Regulink was established by industry veterans, Stuart Reed and Sunil Singh, in 2014, following lengthy independent careers within industry and consultancy organisations. With recent changes to the consulting landscape, Regulink has rapidly grown to take on core partners with highly valuable and niche experience, as well as expanding its consulting partner network to be able to cater for its clients of all sizes. Regulink now offers consulting and other services in UK, Europe, US and Australia, supported by local expertise, and continues to grow, whilst always providing the flexible and scalable services that industry needs.”
Regulink provides specialist consulting and support services in all areas of regulatory affairs, CMC, pharmacovigilance and project/ programme management to the life sciences industry. We have a broad team with relevant experience in the key sectors of this diverse industry.