When subject experts gather, an enterprise inevitably takes shape. Because, then their expertise also joins hands. Mudra Clincare is a result of precisely such a scholarly union. Together, our hold on the subject of toxicology and clinical trials is unrivalled.

The clinical development services we provide can serve the need for both standalone as well as a portion of an integrated full service solution. Besides clinical trials for pharmaceuticals, we focus primarily on medical devices and functional foods.

Why we are different

We consider our ability to attend to the tiniest details by following your smallest requirement, a strength rare in today’s market. We boast of a structure that is capable of delivering a highly personalized service to your clinical development projects.

Why choose us

We recognize the value of time and ease of accessin your business. That is why we prefer to stay awake for you 24X7. Literally. So we are there, at every moment of your critical decision making.Nomatter what time it is, our representatives are always at a phone call away. Mudra Clincare has also created a rapid response email for your facility.

- A young CRO with experience of more than 200 complete clinical development studies. India’s only one to provide all clinical services under a single umbrella.

- A large pool of investigators with in-depth experience in all major and narrow therapeutic areas, and in almost every therapeutic indication, including vaccine studies.

- Cost effective, flexible and dependable services, with a commitment of quality, effective timeline maintenance.

Mudra’s young and innovative leadership, with its experience and expertise, is surging ahead confidently to build a detailed knowledge base that will support our commitment to 24X7 services.

Business Unit Overview

Preclinical

- Clinical development planning

- Regulatory consulting

- Protocol design

- Expert panels

Phase I

- First introduction into man

- PK/PD studies

- Single-dose, multiple-dose, and dose-escalation studies

- Special studies (e.g. food interaction; skin irritation)

Phase II a

- Proof-of-concept studies

- Dose-ranging studies

Phase III

- Large-scale global safety and efficacy studies

- Placebo-controlled studies

- Active-comparison studies

- Bioequivalence studies with clinical endpoints

- Quality-of-life studies

- Resource utilization studies

Registration/Phase III b

- Individual study reports

- Integrated safety and efficacy summaries

- Treatment INDs

- Package inserts

- Submissions in NDA or CTD formats

Phase IV

- Post-approval regulatory commitments/support for primary indication

- New indication studies/labeling expansion

- Medical Information & Professional Contact Center

- Registries and Observational studies.

- Health-related quality of life, patient-reported outcomes via IVRS

- Post-marketing surveillance

- Product Safety and Pharmacovigilance.

- Retrospective chart reviews

- Managed-care studies

- Pharmacoeconomics

Our values

Our group’s values revolve around:

- Assurance

- Expertise

- Smarter approach

Our way of assuring high quality results is maintaining value-focused services with a promise of innovation. And this assurance is backed by essential resources to match the pace of new research trends. We are committed to ensure that every clinical trial that passes our hands is treated with the highest possible standards.

The reputation, earned by Mudra Clincare as one of the most trusted groups in the industry, is by virtue of its proficiency in meeting all clinical needs of our partners. The seamlessness with which our exceptionally competent team takes up the regulatory affairs is a proof of our consummate skill as a clinical consultant.

Recognized for our skilled approach throughout the entire industry, small, midsized, and global pharmaceutical companies look at Mudra Clincare’s customized solutions as a sustainable option that can help meet timelines as well as save considerable costs while accessing highest quality data.

Mission

To provide quality conscious clinical research sites, which are ethical and GCP compliant, in the shortest timelines possible.

History

MUDRA Clincare is on its way to create history. Right now, our only history is the study, research, and vast experience of our team members. It dates back to the time when each of its member labored determinedly to achieve the level of expertise that can help create simplified solutions for their clients when they would come together under the aegis of Mudra Clincare.

Clinical trials in a nutshell

Mudra Clincare stands isthe line of those consultants, which depend heavily on their in-house subject experts and extensive network. What makes it an authority in the field of clinical trials is not just its capability of providing end-to-end solutions, but a mechanism which keeps it updated in real time about every policy change:

1. Approved protocol

2. Investigator selection

3. Approval process

4. Patent recruitment and participation

5. Data entered and reviewed

6. Statistical analysis

7. Presentation and publication of reports

8. Data filed and registration obtained