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BMA is a niche CRO that has been providing functional support in the areas of Data Management and Study Management for over 20 years. Our unique size, coupled with extensive therapeutic experience, allow us to consistently provide personalized, flexible services, and help clients reach critical clinical trial goals and timelines.
Our commitment to our customers and their projects, as well as the consistent quality of our work, are the foundations of our company.
CONFIDENCE – Work with a company whose client base has grown over 20 YEARS, primarily through repeat business and client referrals
EXPERTISE – Gain affordable expertise on your projects with our cross-functionally trained, experienced, and dedicated staff (average of 9 years at BMA and 13 years in industry)
INNOVATION – Expect more than just a CRO and tasks in a contract. Flexible, innovative solutions are the core of our business.
ACCOUNTABILITY – Get what you ask for, when you ask for it. Delivering on promises made, while showing transparency in our actions.
DIVERSITY – Meet your diverse supplier needs. BMA is a WBENC-Certified, woman-owned, small business.
BROAD THERAPEUTIC EXPERIENCE – Biologics, Cardiovascular, CNS, Dermatology, Endocrinology, Gastroenterology, Hematology, Infectious Disease, Musculoskeletal Disease, Nephrology, Oncology, Ophthalmology, Respiratory, Urology, and Women’s Health
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CLINITRIA Ltd. is regionally respected, dynamic and very flexible CRO established by experienced professionals with many years of experience in pharmaceutical development and biomedical research in Western Europe. Company was established in 1995 and it is fully specialized in clinical research since 2002.
CLINITRIA is member of SACROP (Slovak Association of Clinical Research Organizations and Professionals) and EUCROF (European CRO Federation).
CLINITRIA operates in the following Central European countries: Czech republic, Slovakia, Poland, Hungary, Austria and Slovenia. At present we are extending our activities to Romania, Bulgaria and other non-EU Eastern European countries like Serbia, Croatia, and Ukraine, which have relatively short regulatory and EC timelines.
CLINITRIA is able to identify and contract investigators for clinical trials for Phase I - IV studies, identify and contract Pre-clinical Units, perform study setup, monitoring or auditing of clinical trials. We are able to organize investigator meetings and scientific congresses/symposia. Local knowledge is our strong advantage, which allows us selecting the best recruiting investigators, shortening study timelines and obtaining high quality data.
Clinical areas of expertise: cardiology, cardiosurgery, neurology, neurosurgery, psychiatry, oncology, ophthalmology, gastroenterology, endocrinology, rheumatology, pulmonary hypertension, male fertility/erectile dysfunction, etc. We have experience in medical devices studies.
Our activities are strictly based on ICH-GCP guidelines, new EU directives, local legislation and ethical principles.
Scandinavian CRO is a privately held, full service Contract Research Organisation offering both consultancy and specific, stand-alone services. SCRO is head quartered in Uppsala, Sweden and covering Sweden, Norway, Finland and Denmark. We perform complete studies or parts of projects within the field of clinical trials. Both Pharmaceuticals and Medical Device. . If you want to hire a consultant, you can choose between various specialists, such as project managers, clinical research associates, administrators and research nurses.
It is easy to get lost amongst all the national and international laws and regulations governing clinical trials, so it can be nice to sit back and relax in the knowledge that someone is taking care of Good Clinical Practice (GCP) and all the issues related to it. You will naturally always be in control and have oversight of your study, but we are happy to do the work for you, whether you want a consultant or another study specific service.
If you want to use us as an intellectual resource or sounding board, we are happy to share our expertise with you. We can handle phase I to IV clinical trials in a wide range of therapeutic areas: Cardiology, Oncology, Urology, CNS, Endocrinology, HIV, Gastroenterology, Anaesthesia, and many more.
We would love to meet you.
It all begins with a conversation. Contact us.
Phone: +46 - 18 10 05 50
Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. It has been growing at about 25.5% CAGR over the last 5 years and crossed the $1.9 billion mark in the past financial year. The company has set up a network of subsidiaries, under the name Accord Healthcare in EU, US, Canada, SA, Australia, APAC as well as CIS & MENA regions. Intas is present in 85+ countries, with more than 69% of its revenue coming from global business.
Currently ranked 9th in the Indian pharmaceutical market, it’s the largest privately owned Indian generic pharma company. Intas has established leadership in key therapeutic segments like CNS, Cardio, Diabeto, Gastro, Urology and Oncology in India. It is also known for its range of products in other hospital-based therapeutic segments in the EU and US.
Intas operates 15 formulation, R&D and distribution facilities, of which 10 are in India, and the rest in the UK and Mexico. Between them, the facilities are accredited by global regulators such as USFDA, EMA, MHRA, TGA, and others. The company invests ~6-7% of its revenues in R&D and has over 10,000 product registrations worldwide with a strategic pipeline of 300+ high-value FTF/FTM, Biosimilars and NDDS products.
Intas' highly advanced EU-GMP Certified Biopharma division is fueled by a mission to provide affordable “biosimilars for billions” across niche segments such as oncology, auto-immune, ophthalmology, nephrology, rheumatology, and hormone-based therapies.
The Plasma Fractionation Unit of Intas Pharmaceuticals is a pioneer in manufacturing plasma derived therapeutics. It houses a full-fledged R&D lab and a state-of-the-art WHO-GMP certified manufacturing facility complemented with a GLP compliant QC lab.
Our values of Innovation, Customer Delight, Ownership & Collaboration, Performance Focus & Care for Society are the driving forces of our excellence.
Accell Clinical Research is an international full-service Contract Research Organization (CRO) managing Phase I-III clinical trials for 10+ years across Eastern Europe. With local presence, including highly qualified medical staff and legal entities in the region, we successfully recruit patients both in EU and outside EU in post-Soviet countries (CIS). All together we provide guaranteed fast patient recruitment in 20+ countries across the region.
⬇︎ ACCELL'S SERVICES for Phase I-III clinical trials:
• Strategic guidance and trial set-up:
• Feasibility research and site selection
• Study documentation development
• Regulatory support
• Clinical supply import and management
• Selection and management of clinical study vendors
• Project management
• Clinical & medical monitoring
• Data management and biostatistics
• Quality assurance
• Safety management
• TMF/eTMF services
• Functional outsourcing of a clinical team
⬇︎ THERAPEUTIC AREAS