Clinical Trials

“Comprehensive service offerings, tailored to your requirements.”
Our team will bring their expertise and specialized skill sets to your project. We offer a full range of services across a variety of therapeutic areas and guarantee responsiveness and open communication throughout every step.

Our Clinical Trials Services


Project Management
Our project managers take ownership of the project and serve as a single point of contact and liaison between the sponsor, sites and vendors.

Data Management
Our clinical data management team has extensive experience in handling both paper CRFs and EDC- based data management projects. We use a comprehensive 21 CFR Part 11 compliant, commercially available and user friendly data management system.

Medical Writing
Our medical writing team has extensive experience in Protocol Development, Informed Consent, PK/PD Report, Clinical Study Report, Abstracts, IRB Approved patient facing materials, Posters, Regulatory Submissions, and Investigator Brochure development.

Feasibility & Site Selection
Adhering to our streamline process allows us to meet enrollment commitments for your study. We identify the best sites through in-depth research and feasibility .

Clinical Monitoring
Our monitoring services include comprehensive risk-based monitoring plans , source document verification, immediate attention and resolution to issues of protocol noncompliance, remote monitoring, site initiation, interim and close-out visits.

Clinical Quality Assurance
Our clinical quality management team will ensure your study withstands regulatory scrutiny and adheres to FDA Good Clinical Practice compliance guidelines from study inception to database lock.

Clinical Trial Management

ALCHEMY’s clinical trial management services are supported by a highly qualified team of diagnostic and medical device experts. Our proven track record in managing both domestic and international clinical trials from beginning to end sets the foundation of a lineup of industry-leading services. We will fully manage and provide strategic assistance for every phase of your clinical trial. Or, we will provide one or more stand-alone solutions as a functional service provider to complement your internal staff.

  • Study and protocol design and review
  • Case report form (CRF) design and development
  • Informed consent development and review
  • Clinical investigator evaluation, qualification and selection
  • Clinical trial management and coordination
  • Selection, training and management of therapeutically qualified Clinical Research Associates (CRAs)
  • Trial Master File (TMF) creation and management
  • Ethics Committee (EC) submission
  • Medical and safety monitoring
  • Database development and management
  • Sample size calculations, Statistical analysis and review
  • Interim and final reporting
  • GCP audits and training


Herbal And Nutraceutical Services

The expanding Nutraceutical market indicates that end users are seeking minimally processed food with extra nutrition. This development, in turn, is responsible for expansion in the Nutraceutical markets globally. We offer services in designing and conducting clinical trials for herbal and nutraceutical products. We understand the complex issues faced throughout the lifecycle of herbal and nutraceutical products and we offer innovative solutions by integrating our different services. Herbal and nutraceutical products have become increasingly popular in recent years and companies are looking for options to develop products most efficient. As an innovative research organization, we are always seeking for new opportunities to offer our clients the most up-to-date services for herbal and nutraceutical studies.

  • Project Management and Operation
  • Feasibility assessment and site selection
  • Medical Writing -Protocol writing,
  • Clinical investigator evaluation, qualification and selection
  • Clinical trial management and coordination
  • Selection, training and management of therapeutically qualified Clinical Research Associates (CRAs)
  • Trial Master File (TMF) creation and management
  • Ethics Committee (EC) submission
  • Medical and safety monitoring
  • Database development and management
  • Sample size calculations, Statistical analysis and review
  • Interim and final reporting
  • GCP audits and training