Welcome to JSR Pharma Solutions

01 About
Mission

To accomplish our vision by maintaining highest ethical, scientific and quality standards to our Clients and Regulators.

About us

JSR Pharma Solutions is a Quality driven, Consultancy service startup established in 2020. We provide a broad range of Clinical research services to Global Pharmaceutical industry and Clinical Research Organizations.

Vision

To become preferred Clinical research services organization to National and International Global Pharmaceutical companies by complying to National and International regulatory requirements with highest customer satisfaction.

Why choose JSR Pharma

  • Qualified and experienced team who have faced several National and International regulatory inspections.
  • Will consider full approach while formulating strategies in Protocol Development & Finalization, Sample size Determination, Bioanalytical method selection/ alteration, Bio-waiver justification and Data interpretation.
  • Ownership: 100% efforts for the work you have awarded us and will involve completely to ensure that work to be completed within timelines and with quality.
  • Identification/selection of CROs: We have contacts with reputed CROs and hence will help our clients to have smooth communication and transaction.
  • Monitoring expertise: Close monitoring by Subject expert at every important stage of the project to ensure that the project is regulatory compliant.
  • Project management: Dedicated staff to take care of awarded project. Single point of contact, periodic & scheduled telecons
  • Cost saving: we will act you locally on your behalf saving travel and cost.
  • Approach: Consultative and solution oriented.
  • Tailored solutions: We ensure that the system, practices and processes we recommend are aligned with your Organization’s needs.

Our Services

We offer the following services

Leadership

Postgraduate in Pharmacology from College of Pharmaceutical Sciences Manipal.

Brings in 17+ years of experience in Clinical Research domain. Expertise in handling the entire gamut of functions related to Clinical research domain. Experience in handling 500+ Bioequivalence studies and Clinical trials of various dosage forms.

Expertise in Bioequivalence and Clinical trials, Business Development and Project management aspects.

Handled several Regulatory inspections - USFDA, EU, UK MHRA, DCGI, MCC, ANVISA, AFSSAPS etc.

J Ramanjaneyulu
M Pharm Pharmacology

Director