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An Integrated Healthcare Product Development Company
Biovantis is a Healthcare Product development company focused on bringing the high social impact and innovative products and services into the market. Partner with leading GLP compliant Research and Development facilities of India, Biovantis has best in class Inhouse contract research and clinical research services experience and expertise to comprehensive product development solutions to ensure advancement of a candidate products through development, registration and commercial success.

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A Contract Research Organization
As an end to end clinical development company, Biovantis facilitates the product development through various phases of clinical trials. Our clinical development services are compliant with USFDA, MHRA(UK), EMEA (Europe), TGA (Australia) and DCGI (India). Biovantis is focused on reducing expenses, optimizing services and resources to help ensure the quality of clinical research services,

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Pre Clinical Service Provider
Biovantis has inhouse resources to technically manage and conduct the Toxicity studies, Pharmacokinetic and Pharmacodynamic studies, Pharmacology and Genotoxicity studies. All the Preclinical sites are accredited with Good Laboratory Practices (GLP) and follow norms of Organization for Economic Cooperation and Development (OECD) principles by the National GLP and Compliance Monitoring Authority (NGCMA).
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Our Laboratories

Our global laboratories can provide diagnostics solutions for clinical trials across America, Europe and Asia.

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List of Services

9dok services can quickly deliver the information you and your doctor need for your most important health decisions.

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Patronage

With specialist research groups research at 9dok focuses on structural biology and molecular cell biology.

Preclinical Services

Biovantis has unparallel access to the topmost and most reputed Preclinical sites of India to carry out basic research and early development activities for various healthcare product companies including global Biotech, Pharma, Nutraceutical, medical device and Academia institutes. Biovantis has inhouse resources to technically manage and conduct the Toxicity studies, Pharmacokinetic and Pharmacodynamic studies, Pharmacology and Genotoxicity studies. All the Preclinical sites are accredited with Good Laboratory Practices (GLP) and follow norms of Organization for Economic Cooperation and Development (OECD) principles by the National GLP and Compliance Monitoring Authority (NGCMA). Many of the centre are also approved by Department of Scientific and Industrial Research (DSIR), Govt. of India and have CPCSEA approvals.

Clinical Trials Services

Biovantis has a team of highly qualified and experienced Clinical Development professionals with experience across various therapeutic areas and different clinical phases. We can provide a full spectrum of clinical trial services from Regulatory approvals, Protocol development, Ste initiation and monitoring, Clinical Data Management, Pharmacovigilance, Project management and Statistical analysis through Clinical Report Writing and Regulatory submission. Our prior clinical trials experience makes us acutely aware of the critical success factors for project efficiency and demonstrate our ability to implement the appropriate strategies using our technical and operational knowledge of the required ICH GCP trained Investigation sites and patient populations.

Laboratory Services

Clinical Laboratories play a vital role in our day to day operations because they generate a lot of safety data for our products under clinical development development. To ensure that we are always compliant to the global norms of laboratory data, Biovantis only works with NABL and CAP accredited laboratories in India. All the laboratories follow the international guidelines, have fully implemented GLP, stringent internal quality controls and regularly perform external proficiency testing programs. The laboratory partners of Biovantis have PAN India network of collection centers and laboratories to ensure the quick collection and pickup of the laboratory samples of the clinical trials. The laboratories and their logistics partners follow the IATA guidelines while transporting the samples from clinical sites to the central reference laboratories.

ICH-GCP trained Investigators

Biovantis Team has unparalleled access to ICH-GCP trained investigators across different hospitals and research centers in India. Most of the sites have their own research wings with Institutional Ethics Committees which carry out the clinical trials as per the regulatory guidelines and the approved protocols. Biovantis team has experience of managing the sites through its own as well SMO resources tp yield the best results. Our self motivated and dedicated team of doctors has a major role to play in our success and growth and has provided us with an opportunity to deliver outstanding services.

Formulation Development & Manufacturing Support

Formulation Development is another competency of Biovantis which and we routinely carry out development of Generic formulations, Specialty and novel formulations, Consumer and Over-The-Counter (OTC) formulations at our partner sites. .Biovantis develops high social impact healthcare products using innovative technologies and non-infringing & cost effective processes which are scalable to manufacturing level with robust process parameters. .

Project Management & Regualtory Support

Biovantis is built on a strong knowledge base ensuring effective project planning and project implementation. Our specialized experience is focused on the value that India brings to our customers in terms of quality clinical programs conducted by some of the most experienced clinical staff in the country. Members of our leadership team based have previously worked with multinational pharmaceutical companies and clinical research and healthcare companies like Venus Remedies, Reliance Life Sciences, Jubilant Life Sciences, Max Healthcare and Dabur. substantive experience in conducting ICH-GCP studies and studies that fall under the USFDA and European regulations in India and its neighbor countries.

Preclinical Development

Biovantis has unparallel access to the topmost and most reputed Preclinical sites of India to carry out basic research and early development activities for various healthcare product companies including global Biotech, Pharma, Nutraceutical, medical device and Academia institutes. Biovantis has inhouse resources to technically manage and conduct the Toxicity studies, Pharmacokinetic and Pharmacodynamic studies, Pharmacology and Genotoxicity studies. All the Preclinical sites are accredited with Good Laboratory Practices (GLP) and follow norms of Organization for Economic Cooperation and Development (OECD) principles by the National GLP and Compliance Monitoring Authority (NGCMA). Many of the centre are also approved by Department of Scientific and Industrial Research (DSIR), Govt. of India and have CPCSEA approvals.

Clinical Trials Services

Biovantis has a team of highly qualified and experienced Clinical Development professionals with experience across various therapeutic areas and different clinical phases. We can provide a full spectrum of clinical trial services from Regulatory approvals, Protocol development, Ste initiation and monitoring, Clinical Data Management, Pharmacovigilance, Project management and Statistical analysis through Clinical Report Writing and Regulatory submission. Our prior clinical trials experience makes us acutely aware of the critical success factors for project efficiency and demonstrate our ability to implement the appropriate strategies using our technical and operational knowledge of the required ICH GCP trained Investigation sites and patient populations.

Laboratory Services

Clinical Laboratories play a vital role in our day to day operations because they generate a lot of safety data for our products under clinical development development. To ensure that we are always compliant to the global norms of laboratory data, Biovantis only works with NABL and CAP accredited laboratories in India. All the laboratories follow the international guidelines, have fully implemented GLP, stringent internal quality controls and regularly perform external proficiency testing programs. The laboratory partners of Biovantis have PAN India network of collection centers and laboratories to ensure the quick collection and pickup of the laboratory samples of the clinical trials. The laboratories and their logistics partners follow the IATA guidelines while transporting the samples from clinical sites to the central reference laboratories.

ICH-GCP Trained Investigators

Biovantis Team has unparalleled access to ICH-GCP trained investigators across different hospitals and research centers in India. Most of the sites have their own research wings with Institutional Ethics Committees which carry out the clinical trials as per the regulatory guidelines and the approved protocols. Biovantis team has experience of managing the sites through its own as well SMO resources tp yield the best results. Our self motivated and dedicated team of doctors has a major role to play in our success and growth and has provided us with an opportunity to deliver outstanding services.

Formulation Development & Manufacturing

Formulation Development is another competency of Biovantis which and we routinely carry out development of Generic formulations, Specialty and novel formulations, Consumer and Over-The-Counter (OTC) formulations at our partner sites. .Biovantis develops high social impact healthcare products using innovative technologies and non-infringing & cost effective processes which are scalable to manufacturing level with robust process parameters.

Project Management & Regulatory Support

Biovantis is built on a strong knowledge base ensuring effective project planning and project implementation. Our specialized experience is focused on the value that India brings to our customers in terms of quality clinical programs conducted by some of the most experienced clinical staff in the country. Members of our leadership team based have previously worked with multinational pharmaceutical companies and clinical research and healthcare companies like Venus Remedies, Reliance Life Sciences, Jubilant Life Sciences, Max Healthcare and Dabur. substantive experience in conducting ICH-GCP studies and studies that fall under the USFDA and European regulations in India and its neighbor countries.

Contact Us to know how we can help bring your product to the market

Our Registered Office

Biovantis Healthcare Private Limited, Barohal, PO Panchrukhi Tehsil Palampur, District Kangra Himachal Pradesh 176103, India

Our Mohali Office

Biovantis Healthcare Private Limited, SCO -1014, GF, Cannaught Place TDI CITY, Sector 111, Mohali-140307 Punjab India

Our Delhi Office

Biovantis Healthcare Private Limited The Edge Towers, Ramprastha City, Sector -37, Gurgaon-Haryana India .