home - Scientia Bio

The Ideator of A.C.E (Augmenting, Consulting and Enriching) for all Pharma and Biotech Companies.

We are dedicated to being a trusted partner to provide smart and innovative solutions for drug development services with precision & efficacy.

VISION

We are passionate to provide smart and innovative solutions for drug development services with precision & efficacy.

15 Years of Consulting & Training Experience

Empowering organizations with previously unseen insights, enabling them with smarter decision making abilities.

About Scientiabio

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.

Training and Consultation for Pharma and Biotech Companies

Our strength lies on our ability to strengthen our client’s ability to adhere to the best standard of Regulatory body’s guidelines.

TRAINERS

Our trainers have decades of hands- on industry experience to offer the right guidance to your people.

CONSULTATION

Our consultation services offer the best in class advice to boost your company's edge in the market.

OUR SPECIALITIES

Striving towards excellence with a single minded focus to meet and exceed the expectations of our clients, with responsibility & integrity.

Biostatistics

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.

CDISC

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.

Medical Writing

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.

Medical Affairs

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.

Pharmacovigilance

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

Quality and Regulatory Sciences

Our Pharmaceuticals Quality and Regulatory sciences services are categorised in three verticals.
- cGMP Service
- Computer Systems Validation
- Process Scale Up, Validation and Technology Transfer