Veramed Competitors

Quanticate is a leading global data focused clinical research organisation (CRO) primarily focused on the management, analysis and reporting of data from clinical trials and post-marketing surveillance. As experts in clinical data, Quanticate provides high quality teams that offer efficient outsourcing solutions for: • Clinical Data Management • Biostatistics • SAS Programming • Data quality oversight via Centralized Statistical Monitoring • Medical writing • Pharmacovigilance Quanticate can offer study level support, functional service provision (FSP), strategic full data-services solutions or technical consultancy to meet the needs of pharmaceutical, biotechnology and device companies across the globe. Quanticate has become the supplier of choice for many companies from top tier pharmaceutical giants through to niche biotechnology and device companies.

S-cubed Ltd provides professional consultancy services to pharmaceutical and healthcare clients across Europe and the US. Our team of carefully selected consultants and interim managers offers flexible support, ranging from ad hoc advice through to complete project development and implementation. For each project we provide a resourcing solution that is specifically tailored to the client's individual requirements. REGULATORY AFFAIRS With extensive expertise encompassing new chemical & biological entities, generic compounds and therapies for orphan indications, we are ideally qualified to support clients in the formulation of initial regulatory strategy through to registration and beyond. We provide support with agencies liaison and meetings and are well-practised in the writing and management of regulatory submissions. PROJECT MANAGEMENT We provide Project Managers with an in-depth understanding of the operational and tactical requirements for small, large or multiple projects. Our Project Managers have extensive expertise across all aspects of drug development, from pre-clinical to post-marketing activities. QUALITY ASSURANCE Our QA consultants identify and resolve quality issues before they escalate, giving our clients confidence that projects will run smoothly and be in full compliance with the current regulations and guidelines. We can provide support for the development or review of quality systems, SOP writing and training, as well as system, project & vendor audits.

At Richmond, we're on a mission to transform healthcare by delivering faster answers and turning hope into tangible solutions. With over two decades of experience, we've perfected the art of precision, discipline, and innovation in clinical research. Our commitment goes beyond our name – it's a promise to drive progress, elevate patient care, and break down barriers that stand between patients and life-changing treatments. From innovative trial protocols to leveraging our London location and extensive patient database, we're dedicated to making a real impact. Join us in embracing this exciting change. As Richmond, we're shaping a healthier, brighter future, one breakthrough at a time. Stay connected and follow us for updates on our journey of innovation, healing, and hope. #Richmond #FasterAnswers Specialist services: * Early phase adaptive studies including First-In-Human * Cardiac Safety/Intensive ECG/Thorough QT studies * Ethnic Bridging studies * Early phase patient studies (therapeutic and non-therapeutic). Full service: * Consultancy and Expert Advice * Protocol Writing & CRF Design * Regulatory and Ethics Committee Applications * Healthy Volunteer/Patient Recruitment for Phase I-IV * Clinical Conduct, Pharmacy services * Safety Laboratory and Bioanalytical services * Data Management & Statistics and Report Writing