The iLife Pharma Laboratories also provides Chemistry & Manufacturing Control (CMC) consultancy across the spectrum of drug development from early stages to commercialization.

The company was established in 2010 by Prasad and Sons who had previously held senior positions in R and D. iLife Pharma has a multi-disciplinary team of over 20 highly experienced Ph.D. level, senior scientific & technical professionals with backgrounds in pharmaceutical & biotechnology areas. Collectively, iLife Pharma possesses over 400 years of CMC experience and expertise.

Our Team, Strength & Approach

Our Team

Our team consists of over 25 senior scientific and technically proficient professionals. This team has collective experience and expertise in the following:

CMC R&D activities and commercial Manufacturing operations.

Pharmacokinetics and Biopharmaceutics.

Many Pharmaceutical Companies (including Multi-nationals), Universities and Regulatory Agencies (FDA, MHRA).

Drug development with many products, including blockbusters, successfully filed and approved with Regulatory Agencies.

Our Strength

We have a wide knowledge and experience working with Contract Research (CRO's) and Contract Manufacturing Organisations (CMO's) .This enables us to provide:

Identification of appropriate CMC Development laboratories and GMP Manufacturing capabilities.

Assessment of emerging CRO's and CMO's under consideration by the client.

The level of scientific and technical expertise available at specific companies.

Assessment of regulatory competence.

Value and reliability.

Our Approach

We are able to provide the right expertise and experience for your project.

Close interaction with each client to fully understand the project scope.

Provide a customised solution for each project to deliver efficiently and effectively.

Highly responsive and cost conscious to provide value and quality to meet each client’s expectations.