At CRC Pharma, a clinical research and reporting organization, we are constantly striving to bring better patient care by facilitating and supporting translational clinical development programs. CRC Pharma, is a rising Clinical Research Organization (CRO) in New Jersey, exclusively focused on supporting clinical and translational development programs spanning from very early on to late stage developments. We provide both operational and consulting services to our esteemed clients who aspire to develop safe and efficacious new drugs, devices and biologicals.

Our core strength is in biostatistics, statistical programming and data management involved in clinical drug trials. We are also providing expert and efficient services in the area of medical, clinical and regulatory affairs, clinical trial disclosure, pharmacokinetic and pharmacodynamic (PK/PD) analysis and pharmacovigilance.

Our work has gained us recognition and respect amongst the peers and stakeholders, as it sprouts from extensive scientific acumen and over 200 years of cumulative experience. We have been consistent in delivering high quality services for various therapeutics areas.

WHAT WE DO

OPERATIONAL SERVICES

  • Biostatistics
  • Clinical / statistical programming
  • Clinical data management
  • Transparency in clinical trials
  • Medical and regulatory writing
  • Clinical PK and PK/PD data analysis
  • Pharmacovigilance

STRATEGIC CONSULTANCY SERVICES

  • Planning for early stage clinical development programs
  • Strategic inputs in regulatory submissions e.g. IND, BLA, ANDA
  • Clinical and regulatory support
  • Expert advice on CDISC data review and compliance to US-FDA
  • Advice on plan, design and execution of nutraceutical products

TRAINING SERVICES

  • Basic and advanced : Good Pharmacovigilance Practices (GPV)
  • Clinical SAS programming
  • Art and science in writing clinical lay language summaries

OPERATIONAL SERVICES

  • Biostatistics
  • Clinical / statistical programming
  • Clinical data management
  • Transparency in clinical trials
  • Medical and regulatory writing
  • Clinical PK and PK/PD data analysis
  • Pharmacovigilance

STRATEGIC CONSULTANCY SERVICES

  • Planning for early stage clinical development programs
  • Strategic inputs in regulatory submissions e.g. IND, BLA, ANDA
  • Clinical and regulatory support
  • Expert advice on CDISC data review and compliance to US-FDA
  • Advice on plan, design and execution of nutraceutical products

TRAINING SERVICES

  • Basic and advanced : Good Pharmacovigilance Practices (GPV)
  • Clinical SAS programming
  • Art and science in writing clinical lay language summaries

CRC PHARMA INSIGHTS

We provide innovative, organic solutions with holistic approach

We engage in project specific personal interaction with clients and help generate scientific and rationale solutions

Implement “Team Science” approach from concept to client satisfaction

Consistent high quality is our signature mark

Our team of subject matter experts capable of delivering transformative scientific outcomes

We have earned high market/client trust, credibility and industry connections due to our quality of work

We provide innovative, organic solutions with holistic approach

We engage in project specific personal interaction with clients and help generate scientific and rationale solutions

Implement “Team Science” approach from concept to client satisfaction

Consistent high quality is our signature mark

Our team of subject matter experts capable of delivering transformative scientific outcomes

We have earned high market/client trust, credibility and industry connections due to our quality of work

STRIVING FOR PATIENT CARE & CLINICAL DEVELOPMENT PROGRAMS