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Pharmadesk Solutions Private Limited

Navi Mumbai, Maharashtra

| GST  27AAFCP9660F1Z4

| Verified Supplier

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Pharmadesk is one of the leaders in providing end to end solution for all the BE related requirements of generic pharmaceutical companies. It supports complete BE study requirements, conduct and management aspects through a portfolio of well-designed services.   We work with a well-defined goal: To work closely with our clients and respective service providers as a ligament ensuring that the projects are delivered within stipulated timelines at accurate price and being technically competent to face regulatory challenges.   After years of contribution in various leading Generic Pharmaceutical companies, Dr. Ravindra Bhavsar identified the specific needs of product developers, which need expertise beyond what typical CROs can offer. The idea of Pharmadesk germinated with this thought and was started in the year 2011. During the last 07 years, we gradually became a solid platform for some of the most complex generic developments in most of the developed markets by providing BE related support and are driven by a dedicated team of more than 25+ like-minded industry experts. Pharmadesk now boasts the capability to support the Bioequivalence requirements for various dosage forms ranging from oral solids to complex injectable products and markets. We have been successfully delivering solutions to many multinational generic companies focusing on USFDA, MHRA TGA, Canada, Brazil and many more submissions.+ Read More

Nature of Business

Consultants

GST Number

27AAFCP9660F1Z4

Monitoring Bioequivalence Study Services
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Dosage FormSyrup, Tablets, Capsules, Injection, Creams/Ointments
Durationdepend on customer
Locationall over world
Product TypeAPI
Service Chargesdepend on customer

Pharmadesk is providing consulting & complete project management services to generic pharmaceutical companies for Bioequivalence and related activities. We have been supporting Generic Pharmaceutical companies in Product feasibility assessment, CRO selection, Medical writing, Project management for BE study, BE study monitoring, Failed BE study analysis, IVIVC and Regulatory support regarding BE studies.

Our strength is our technically sound team who have been constantly delivering the projects within time. We provide a deep insight to your generic product development and ensure a risk mitigation strategy is in place for bioequivalence program to save millions of dollars for your organisation.

With 25+ experienced & qualified team of Project Managers, Clinicians, Pharmacologists, Formulators, QA, Regulatory, Analytical, Bioanalytical experts as well as Ex-MHRA Consultant on Board, Pharmadesk takes complete ownership of your Bioequivalence studies and ensures they get completed efficiently & successfully by carefully evaluated & selected CROs in India.

With an experience of handling more than 380 successful BE studies submitted to EU and USFDA regulatory authorities and based on the cumulative experience of multiple products for multiple markets, we have well-defined processes in place for every activity in the Bioequivalence study cycle. We assign a dedicated project manager for every project to ensure complete attention is given to individual projects.

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Consultancy for Bioequivalence Study monitoring
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Durationdepend on customer
Dosage FormCreams/Ointments, Tablets, Capsules, Injection, Syrup
Product TypeAPI
Locationall over world
Service Chargesdepend on work

Pharmadesk provide end to end bioequivalence services to our clients, start from product feasibility to report submission and till responding regulatory queries. Our services include complete bioequivalence project management, CRO qualification & selection, design and conduct of bioequivalence studies, medical and regulatory writing services, failed biostudy investigations, clinical and bioanalytical review etc.

 

As Generic Pharmaceutical industry continues to mature and penetrate new areas, the regulatory and competitive landscape becomes more challenging. Every stage of the product life cycle needs very specific expertise and detailed understanding. Bioequivalence (BE) being one of the most important aspects of the generic product development, has always gained significant attention from the Regulatory Authorities throughout the world.

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Bioequivalence Study Services
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Dosage FormCreams/Ointments, Capsules, Syrup, Tablets, Injection
Durationdepend on customer
Product TypeAPI
Locationall over world
Service Chargesdepend on work
UsageClinical

Pharmadesk is providing consulting & complete project management services to generic pharmaceutical companies for Bioequivalence and related activities. We have been supporting Generic Pharmaceutical companies in Product feasibility assessment, CRO selection, Medical writing, Project management for BE study, BE study monitoring, Failed BE study analysis, IVIVC and Regulatory support regarding BE studies.

 

Our strength is our technically sound team who have been constantly delivering the projects within time. We provide a deep insight to your generic product development and ensure a risk mitigation strategy is in place for bioequivalence program to save millions of dollars for your organisation.

 

With 25+ experienced & qualified team of Project Managers, Clinicians, Pharmacologists, Formulators, QA, Regulatory, Analytical, Bioanalytical experts as well as Ex—MHRA Consultant on Board, Pharmadesk takes complete ownership of your Bioequivalence studies and ensures they get completed efficiently & successfully by carefully evaluated & selected CROs in India.

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Experienced on Conducting Bioequivalence Study Consulting Company
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LocationIndia

Pharmadesk is providing consulting & complete project management services to generic pharmaceutical companies for Bioequivalence and related activities. We have been supporting Generic Pharmaceutical companies in Product feasibility assessment, CRO selection, Medical writing, Project management for BE study, BE study monitoring, Failed BE study analysis, IVIVC and Regulatory support regarding BE studies.

Our strength is our technically sound team who have been constantly delivering the projects within time. We provide a deep insight to your generic product development and ensure a risk mitigation strategy is in place for bioequivalence program to save millions of dollars for your organisation.

View Complete Details

Yes I'm interested

Medical Writing
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Medical Writing

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Mode of ServiceOnline
Service TypeMedical Writing
LanguageEnglish, Hindi
IndustryPharmaceutical
Type of Service ProviderIndividual, Company

Medical Writing

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Are You Looking for CRO\'s for BE Study
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Dosage FormSyrup, Tablets, Creams/Ointments, Injection, Capsules
Product TypeAPI
UsageCommercial

Pharmadesk is one of the leaders in providing end to end solution for all the BE related requirements of generic pharmaceutical companies. It supports complete BE study requirements, conduct and management aspects through a portfolio of well-designed services.

 

We work with a well-defined goal: To work closely with our clients and respective service providers as a ligament ensuring that the projects are delivered within stipulated timelines at accurate price and being technically competent to face regulatory challenges.

 

After years of contribution in various leading Generic Pharmaceutical companies, Dr. Ravindra Bhavsar identified the specific needs of product developers, which need expertise beyond what typical CROs can offer. The idea of Pharmadesk germinated with this thought and was started in the year 2011. During the last 07 years, we gradually became a solid platform for some of the most complex generic developments in most of the developed markets by providing BE related support and are driven by a dedicated team of more than 25+ like-minded industry experts. Pharmadesk now boasts the capability to support the Bioequivalence requirements for various dosage forms ranging from oral solids to complex injectable products and markets. We have been successfully delivering solutions to many multinational generic companies focusing on USFDA, MHRA TGA, Canada, Brazil and many more submissions.

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Yes I'm interested

Scientific Writing
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Scientific Writing

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Service TypeMedical Writing
IndustryPharmaceutical

Scientific Writing

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