Since 1994 MZD is valued as long-lasting and reliable partner in providing clinical research professionals for clinical trials for the pharmaceutical, medical device & biotech industry. With a steadily expanding network of highly qualified freelance clinical research professionals MZD is specialized in project based staffing solutions for phases I through IV.
MZD also offers recruitment support for permanent staffing vacancies where we search for highly qualified and motivated professionals and executive staff.
Regulatory and Quality Solutions, LLC (“R&Q”), is an ISO 9001:2015 certified consulting firm that provides comprehensive global regulatory affairs and quality assurance expert implementation services to the Medical Device Industry.
R&Q has advised more than 250 clients across more than 1,000 projects with a diverse array of service offerings including, but not limited to: regulatory affairs, quality systems, clinical evaluations, design assurance, product quality, large remediations, and post-market surveillance.
R&Q has successfully partnered with clients of all sizes, from startups to large multinational firms, and across all modalities and classes of medical devices – nationally and internationally. R&Q has emerged as a partner to 13 of the top 20 global medical device companies by offering business balanced solutions to solve complex quality and regulatory issues in areas such as FDA medical device regulations, EU MDR, MEDDEV 2.7/1 Rev 4, ISO 13485:2016, and MDSAP.
Created in 1990, Strategie Sante is an independent French company providing Assistance and Advisory services to Pharmaceutical Laboratories with full confidentiality.
Thanks to our proven expertise in Regulatory Affairs, Pharmaceutical Development, Project Management, Medical Devices, Quality/Audits and Market Access, we support our clients throughout all steps of the conception and lifecycle of their products ensuring a complete quality service.
MedPharm is the world’s leading contract provider of topical and transdermal product design and formulation development services. MedPharm is experts at reducing risk and accelerating development times for generic and proprietary pharmaceutical customers through their unique, cost-effective and industry-leading performance testing models.
Well established as the global leaders in dermatology, nail, mucosal membrane, and transdermal product development, MedPharm can also offer innovative solutions for ophthalmic and airway preparations recognised for their scientific rigour by regulators and investors. MedPharm has fully established Centers of Excellence in the USA and the UK.
Ancillarie is a support services company established in 2012. The company provides services in Biostatistics, Clinical Data Management, Medical Writing, Pharmacovigilance, Resourcing, and Quality Assurance services for Pharmaceutical, Biotechnology, and Contract Research Organizations and helps them to accomplish their goal.
Trials24 accelerates online patient recruitment for clinical trials worldwide, helping CROs and biopharmaceutical companies find patients their sites can’t reach.
We reduce our customers’ recruitment time by 6 months or more, with a return on investment (ROI) of 7-12x, providing 20-65% of all randomized patients. With an inbound call acceptance rate higher than 90% and an average of 4 to 11 touchpoints per patient, our country-specific Patient Companion Service ensures high-quality participant selection and high patient engagement rates in various therapeutic areas.
Trials24 offers Patient-Reported Feasibility Studies based on real-world data (RWD) to ensure online recruitment success, cost predictability, and timeline consistency. We build a recruitment cost model that projects patient enrollment costs by measuring the patient population’s eligibility rate specifically to the study protocol. Our RWD-based scientific approach assures our clients that our campaign will be ROI-positive before implementation.
PLUS ANALYSIS is an independent analysis and consulting company specializing in clinical trials and post-marketing studies. Our senior staff has experience in data management, data analysis and data presentation. PLUS ANALYSIS provides independent, top-tier data management and consultancy services, ensuring the integrity, reliability, and efficiency of every project we undertake. With our experienced team, we provide essential steps in statistical data analysis such as sample size calculation, randomization setup, paper Case Report Form (CRF) design, protocol review support, and Statistical Analysis Plan (SAP) development. Our expertise extends to creating databases, double data entry, cross-checking, and managing queries with tailored solutions. We strengthen your projects with our proficiency in generating interim and final analysis reports, crafting clinical study reports, creating customized tables, graphs, and listings, and offering statistical interpretation of study results. We are an ambitious company in terms of cost and quality and are here to collaborate with customers for achieving scientific success.
The Science Behind combines neuroimaging and neurostimulation technologies with tailored services specifically for Phase I clinical trials for CNS indications. Our expertise provides a crucial advantage for Sponsors and CROs, enabling them to de-risk future pipeline decisions and enhance their neuroscience capabilities.
Through our state-of-the-art technologies and access to world-leading neuroscientists, we ensure every project benefits from the latest science and multidisciplinary collaboration.
We focus on efficiency and data insights. Our integrated approach of technology and flexible service model, allows us to deliver custom solutions anywhere and anytime, seamlessly integrated into complex clinical trial designs. This approach efficiently provides clients with objective insights to drive early decision-making and enhance trial management.
We are dedicated to offering innovative solutions that meet the evolving needs of Phase 1 clinical trials. Let us guide you through the complexities of CNS clinical trials with our expertise, cutting-edge technology, and commitment to excellence.
Reguclin Consulting provides a comprehensive Medical Affairs and Clinical Development function tailored for the pharmaceutical and biotech companies. Our strategic drug development solutions encompass global preclinical and clinical design for a variety of products, including differentiated drugs, complex generics, biosimilars, novel biologics, advanced therapies, and vaccines. As a specialized consultancy, we offer a wide range of services across all stages of the product life cycle—predevelopment, preclinical, clinical, dossier review, and post-authorisation. Our expertise spans clinical development strategy and execution for various medicinal categories, dosage forms, and therapeutic segments, ensuring smooth regulatory submissions worldwide. We also excel in new product identification, end-to-end medical writing, and pharmacovigilance solutions, including EU QPPV services. By leveraging our innovative clinico-regulatory approach and extensive experience with global healthcare authorities, we collaborate closely with you to streamline your product development process. This partnership enhances your organization’s efficiency and maximizes the value of your regulatory filings, paving the way for a successful market launch.
Cureline Baltic is a preclinical CRO, specializing in oncology, autoimmune and microbiota research Our services include broad spectrum of in vivo and in vitro studies, such as toxicology, bioavailability, bioequivalence, as well as PD/PK, MTD and efficacy testing. Cureline Baltic is advancing a novel double cellular barcoding technology – MetTrackerTM – designed to monitor the impact of drugs on primary tumors and metastasis on mice at a single cell level.
