Biolidics Limited (Formerly known as Clearbridge BioMedics)

Advanced BioScience Laboratories, Inc (ABL) is a leading contract research and manufacturing organization, that partners with our clients to support their vaccine and therapeutic development programs. We offer a unique combination of preclinical and clinical services designed to first address the scientific challenges often encountered during proof-of-concept, and then streamline process development and cGMP production of clinical supply.
ABL can assist with all aspects of production development including, but not limited to:
Basic and translational research
Vaccine and therapeutic product design
Animal models for preclinical evaluation including immunomonitoring , efficacy and potency
Cell line and process development
cGMP manufacture of cell banks and virus banks
cGMP manufacture of clinical supply for protein therapeutics, vaccines and live viral vectors

Ask about our 9,000 sq ft clinical GCLP immunomonitoring space and our vaccine and therapeutic testing services.

With a 50+ year history as a service provider to the life sciences industry, ABL brings a broad technical knowledge base, highly experienced work force, and seasoned project management to every program. Our goal is to become a seamless extension of our clients’ product development group – helping them advance today’s ideas into tomorrow’s medicines. Our history, capabilities and expertise allow ABL to provide solution based services to our clients.

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
• Oncology
• Cardiovascular
• Immunology
• Gastroenterology
• Neurology
• Endocrinology

ACI Clinical provides advisory services to solve complex issues in clinical research. We specialize in clinical and safety consulting, including full service Endpoint Adjudication Committees and Data Monitoring Committees. By leveraging our in-house experts and biostatistical staff with our global network of over 550 medical experts, ACI Clinical is able to provide our clients with high-value solutions that enhance trial integrity and prepare client data for publication, submission, and approval. Our clients receive the latest scientific and regulatory thinking due to our executive team’s constant involvement in private-public thought leadership efforts focused on establishing best practices. In addition, ACI's in-house team has more committee experience per person than anywhere else in the industry, and our proprietary adjudication technology, AIMS™, has been recognized as the best in the market. Since 2001, ACI has managed projects for hundreds of different pharmaceutical, biopharma, device, biotech and non-profit association clients in virtually every therapeutic area around the world. Our commitment to performance excellence has helped us to support 30 product approvals and numerous publications, with a near 90 percent rate of repeat business.

Our vision is to conduct clinical trials better and more cost effectively than anyone else. We accomplish this by working with our clients to not only deliver the clinical trial effectively, on time and within budget, but also by leveraging our in-depth expertise to ensure the clinical trial is properly designed.

We believe there is increasing need for innovation, creativity and scientific expertise in clinical research, characteristics often synonymous with small Biopharma and hence, though we are proud to have a number of the world’s largest pharmaceutical companies as our clients, greater than 80% of our client portfolio is small Biopharma.

ACLIRES has performed trials for an international array of biotech companies as well as for some of the largest global pharmaceutical companies. With our broad access to patients and expertise, our aim is to rapidly initiate our client’s studies, even when a very special patient population is required.

Our services include:
- Early Phase Studies
- Late Phase Studies
- Recruitment
- Regulatory Affairs
- Monitoring
- Site Selection
- Scientific Services/Medical Writing
- Consulting
- Quality Management

Actimus Bio is an Clinical Research Organisation (CRO)

 Actimus Bio is pioneering a novel approach by addressing the needs of the pharmaceutical and biotech industry and partnering the development of medicines for the future.
 Actimus Bio facility is approved by Drugs Controller General of India (DCGI).
 Actimus Bio is a full service BA/BE CRO dedicated to meet the needs of pharmaceutical and biotechnology companies.
 Actimus Bio offers an extensive range of Clinical services including
o Study design,
o project management,
o Medical safety monitoring,
o Biostatistics,
o Quality assurance auditing,
o Regulatory submissions and scientific communications