PharSafer® February Newsletter

Balti-more Insights From Events

At the recent DIA GPVRMS Conference in Baltimore, USA PharSafer® delved into the challenges and strategies for integrating automation in drug safety, speaking on the topic of Empowering Transformation: Tackling Concerns in Implementing Automated Safety

Solutions, highlighting the necessity for both regulatory compliance and organizational understanding of what automation needs to achieve. This conference provided an invaluable platform for networking, allowing us to exchange ideas and experiences that reinforce our commitment to leading the industry towards a (Phar)Safer, more efficient and accurate future in drug safety processing.

As PharSafer® continues to embrace innovation, we are inspired by the collaborative spirit and shared goals evident amongst our industry peers, furthering our mission to ensure the utmost safety of medicines worldwide through compliant and accurate safety data capture.

Schedule a meeting with Dr. Graeme Ladds

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Jumpstart Your Journey with R.A.P.T.A.R®!

In our continuous effort to provide unparalleled cost-effective solutions and support to our clients, PharSafer® is thrilled to announce an exclusive promotion for our new and existing clients that is certainly not to be missed!

For a limited time only, use the code #RAPTAR2024 when booking your introductory call, and unlock a suite of complimentary benefits designed to seamlessly integrate our automated services into your safety operations.

What's Included?

  • Free Implementation: Kickstart your journey without the upfront costs – we'll set up everything you need and guarantee a smooth transition.
  • 3 Months Complimentary Processing: Experience our industry-leading services with THREE MONTHS of processing on the house. It's the perfect way to witness the impact of our expertise on your safety processing projects.
  • Follow-Up Reports: Gain valuable insights with follow-up reports, provided at no cost, to enhance your data quality and understanding of our impact together on safety case processing.

From clinical trial support to post-marketing surveillance, our tailored solutions are designed to combine automation and accuracy to advance your projects with precision and care.

This offer is reserved for the next 10 sign-ups only, so act quickly!

Use code #RAPTAR2024 when booking your introductory call and be one of the lucky 10 to secure these unparalleled benefits.

Book Your Introductory Meeting Today!

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Our New Website is Launching Very Soon!

We're excited to announce the upcoming launch of PharSafer's new website, designed to enhance your experience with updated service information, latest company news, and insightful regulatory updates!

To further highlight our commitment to providing first-class support to our clients, our website will introduce our brand-new PharSafer® One-Stop-Shop – allowing our clients to easily select and tailor the services they require, from clinical trial support to regulatory consulting and product launch activities, to ensure they achieve end-to-end compliance.

This significant update aims to provide further clarity and transparency to the process of identifying your requirements, whilst also streamlining the process to ensure work can begin as soon as possible, and keep you well-informed and ahead of the industry curve.

Stay tuned for the official launch announcement coming very soon – and prepare to explore a wealth of capabilities crafted with your needs in mind!

Graeme Ladds, CEO

With a first degree in Biochemistry and Pharmacology and a PhD focusing on drug metabolism and Pharmacokinetics, Dr. Graeme Ladds has worked in the areas of Drug Safety and Medical services for over 30 years.

Working as a Head of Global Pharmacovigilance for a multi-national innovator Company and EU QP PV for several of the top ten Pharma Companies, large generic and smaller innovative Pharma,

Graeme is the CEO and Owner of

PharSafer® – a position held for the last 21 years – and he has taken many products from bench to clinical to post-marketing in many global markets; helping many small start-up Companies (Biotech, Advanced Therapy, Medical Device, Biologic, Generics, Herbal, OTC) in their planning and growth, due-diligence activities for product in-licensing and marketing, and development strategies with partner and distributor Companies. Graeme has also been involved in many global audits (conducted) and inspections (taken part in) for clients and also database designs and development.

Contact Dr. Ladds
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