Actimus Biosciences Private Limited | Company Profile
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Keywords & Focus Areas
Actimus Biosciences Private Limited
Overview
Actimus Biosciences Private Limited is a Contract Research Organization (CRO) based in Visakhapatnam, India, established in 2005. The company specializes in comprehensive drug development services for pharmaceutical and biotechnology companies around the world. Actimus focuses on clinical research and bioanalytical services, emphasizing innovation, integrity, and customer service.
The company offers a wide range of clinical research services, including study design, project management, medical safety monitoring, biostatistics, quality assurance auditing, and regulatory submissions. It is particularly known for its Bioavailability/Bioequivalence (BA/BE) studies, conducted in FDA-approved facilities equipped with 138 beds, ensuring compliance with international standards. Serving a global clientele and partnering with industry leaders, the organization is committed to delivering high-quality services while fostering an agile and socially responsible research environment.
Basic Information
Industry | pharmaceuticals |
---|---|
Founded | 2005 |
Revenue | 10M |
Headquarters | 93 sunnyvale court, Visakhapatnam, Andhra Pradesh, India |
Languages | English |
Contact Details
- Phone: +91 89166 72000
- Website: actimusbio.com
- LinkedIn: linkedin.com/company/actimus-biosciences-private-limited
Key Focus Areas & Initiatives
- Contract research organization services
- Pharmaceutical development
- BA/BE studies
- Pharmaceutical manufacturing
- Analytical services
- Clinical trial management
- Bioanalysis for biologics
- Data management
- Toxicology analysis
- Medical laboratories
- Bioanalytical assay development
- Bioequivalence studies
- Regulatory submissions
- PK & statistical services
- Method validation
- PK & PD analysis
- Bioanalysis for biotech
- High sensitivity analysis
- Sample analysis
- Clinical research
- High throughput analysis
- Bioanalytical SOPs
- Regulatory documentation
- Analytical method validation
- GLP compliance
- Bioanalytical services
- Bioanalytical methods
- Data integrity
- Bioanalytical for complex molecules
- Sample storage in freezers
- Regulatory compliance
- Bioanalytical assay validation
- Bioanalytical for high volume samples
- Bioanalytical research
- FDA-approved facilities
- Medical writing
- Biopharmaceutics
- Quality control
- Regulatory standards
- Pharmacokinetics
- Toxicology testing
- Bioanalysis for generics
- Pharmacovigilance support
- LC-MS/MS
- Pharmacology services
- Patient population studies
- Laboratory services
- GLP laboratories
- Biotechnology
- FDA compliance
- Bioanalytical for veterinary drugs
- Bioanalytical testing
- CRO services
- Regulatory approval
- Bioanalytical for challenging matrices
- Sample handling
- Bioanalytical laboratory
- Bioanalysis for first-to-file projects
- Clinical sample analysis
- Bioanalytical method transfer
- Preclinical bioanalysis
- Drug development support
- Regulatory inspections
- Bioanalytical method development
- Sample storage facilities
- Preclinical studies
- Toxicokinetics
- Bioanalysis for biosimilars
- Bioanalysis for small molecules
- Clinical trial support
- Sample storage
- Validation protocols
- Toxicology studies
- B2B consulting
- Research and development in the physical, engineering, and life sciences
- Customer service
- Risk assessment
- Medical innovation
Technologies Used
- AI
- Apache
- Bootstrap Framework
- Google Font API
- Microsoft Office 365
- Mobile Friendly
- Outlook