APCER Life Sciences provides comprehensive drug safety/pharmacovigilance, medical information, medical writing, regulatory services, quality assurance and risk management programs to pharmaceutical and biotech companies globally.
We bring medicinal / scientific expertise through our healthcare professionals & physicians and address full pharmacovigilance requirements for North America, UK & Europe markets. Our clients benefit from our vast experience in regulatory submissions across 100+ countries and consultative approach towards audit /inspection readiness.
Our focus towards Patient safety and Risk profile management makes us the preferred choice for pharma companies who are looking for pre /post marketing compliance & reporting solutions.
We have scalable operations across five global offices which house more than 750 employees: Princeton, NJ, USA; London, UK; Germany, Wan Chai, Hong Kong, New Delhi and Ahmedabad, India.
We are an established all-phase contract research organization (CRO) based in Berlin, Germany.
We provide complete turn-key solutions for all stages of the clinical development process, including data management, biostatistics, clinical and medical monitoring as well as medical writing and pharmacovigilance services.
We are involved in several global clinical trials and – through collaboration with strong partners – has established a position at the forefront of the latest developments in the world of clinical research. We can manage complete clinical projects from initial trial inception through to regulatory submission.
Our experienced team has substantial expertise in the various divisions of clinical research which enables the company to offer services from preclinical to phase I-IV and post-marketing studies for pharmaceutical, biotech and medical device companies.
OCT is the leading contract research organization in Russia. Since 2005, OCT’s team has conducted over 300 clinical trials in Eastern Europe and the CIS region. Our team of 150+ clinical professionals provides a full range of high-quality CRO services for Phase I-IV and BE studies, with therapeutic expertise in oncology, infectious disease, and all major therapeutic indications.
As pharmaceutical and biotechnology companies have turned toward outsourcing models in clinical research, OCT has established itself as one of the top contract research organizations worldwide. With strong local expertise and focus on quality, OCT ensures seamless clinical trial conduct and drug registration, on time and within budget.
Our experienced team delivers a full range of CRO services:
Clinical Study Design Preparation
Consulting and Regulatory Support
Project Management and Monitoring
Drug Safety and Pharmacovigilance
Clinical Supply Services and Logistics
GMP Inspection Support
DataClin is a Contract Research Organization (CRO) in Egypt focusing on Clinical data management, Bio-statistics, Medical writing, Clinical monitoring, pharmacovigilance, Consultancy, and training services.
We, at DataClin, work according to a full set of standards covering our scope of work, with an ongoing process of updates as per international, regional, and local regulatory requirements and guidelines with full respect to customer-specific standards.
We commit ourselves to excellence, focusing on people development, and are able to perform clinical research projects, spanning across various therapeutic areas, while delivering high-quality output.
DataClin is able not only to reach our partner expectations; yet exceeding those expectations from all perspectives.
DataClin team aims to grow together with our customers always demanding the highest standard of professionalism and integrity of ourselves with a commitment to consistent quality and execution.
DataClin team has extensive experience that captures the full workflow of Clinical Data Management, Biostatistics and Medical Writing and Clinical Monitoring processes on all phases of clinical trials as well as post-marketing registries.
We have a wide experience in multinational pharmaceutical business having experience with most of the top 10 multinational companies.
Marti Farm Ltd, company based in Zagreb, Croatia is a CONTRACT RESEARCH ORGANIZATION supporting the needs of the pharmaceutical, biotechnology, medical devices, food supplement and cosmetics industries across a variety of core services areas. We are internationally recognized as a reliable partner and provider of consultancy and regulatory services with proven track record of 8+ years. Our core belief is continuous personal development aimed at strengthening our expertise and approaches in order to drive added value for our clients from both the operational and the strategic aspects. Over the last several years, we have been increasingly expanding our business internationally in search for new satisfied clients and trusted partners.
Our core service areas:
EU QPPV, Local QPPV, operational
• Pharmacovigilance in clinical trials
• Medicinal products and medical devices
• Cosmetic products
• Food supplements
• RUT/PIL & bridging report
• We offer full services for conducting clinical trials with individual approach to each client so we can offer service at every stage of the trial (phases I, II, III and IV).
• We offer medical writing services in the field of pharmacovigilance and regulatory affairs.
• We provide you with accurate translations made by experienced language experts.
PATIENT SUPPORT PROGRAMS
• We in Marti Farm rise up to the challenge by giving the patients access to the support they need while ensuring healthcare utilization.
• Our certified teams will help you establish a QMS and guide you through audits.
• Our medical marketing team would love to become your partner and guide through the ever-evolving landscape of medical communications and publications.
HEALTH ECONOMICS AND MARKET ACCESS
• HE Analyses
• Pricing, reimbursement & market access