We are dedicated to being a trusted partner to provide smart and innovative solutions for drug development services with precision & efficacy.
We are passionate to provide smart and innovative solutions for drug development services with precision & efficacy.
Empowering organizations with previously unseen insights, enabling them with smarter decision making abilities.
ScientiaBio, is young and energetic Indian CRO (established on March 2010), with a global client base, is a dominant player to the Phama Emerging Nations. We provide precise and targeted solutions to different areas of pharmaceutical development primarily for small & medium size companies.
Our cutting age consulting & training services empower organization with previously unseen insights, enabling them with smarter decision making abilities. Our strength lies on our ability to strengthen our client’s ability to adhere to the best standard of Regulatory body’s guidelines.
Our strength lies on our ability to strengthen our client’s ability to adhere to the best standard of Regulatory body’s guidelines.
Our trainers have decades of hands- on industry experience to offer the right guidance to your people.
Our consultation services offer the best in class advice to boost your company's edge in the market.
Biostatistics is necessary to prove the effectiveness in clinical studies and reduce the cost of drug development. Our highly experienced and expert statisticians provide insights and perspectives that’s aids to simplify clinical development and execute it seamlessly.
Clinical Data Interchange Standards Consortium (CDISC) has provided extensive guidelines for the collection, analysis and submission of clinical trial data for regulatory compliance purpose. Submitting data compliant with CDISC is mandatory for new drug development.
The success of a meticulously done research and tenaciously conducted clinical trial depends on a large extent to the well structured scientific & regulatory document presented to the regulatory authority.
ScientiaBio, since its inception has worked with large and small biotech and pharmaceutical companies to shape their commercial growth success from market access planning to post launch growth.
Ongoing monitoring of product and patient safety is of paramount importance from the earliest stages of pharmaceutical development and throughout the product life cycle. Our team of expert PV consultants
Our Pharmaceuticals Quality and Regulatory sciences services are categorised in three verticals.
- cGMP Service
- Computer Systems Validation
- Process Scale Up, Validation and Technology Transfer