Oversight
Precision Monitoring, Proven Results
Haleus excels in clinical monitoring, ensuring each trial meets stringent standards with precision oversight. Our experienced monitors adeptly navigate complex regulations and challenges, driving trials toward successful outcomes.
Study Start-Up
- Identifying and setting up sites: Selecting optimal locations and preparing facilities for clinical trials.
- Securing regulatory and EC approvals: Navigating the approval process to meet ethical and regulatory standards.
- Finalizing agreements: Drafting and executing contracts with all trial stakeholders.
- Initiating sites: Launching clinical operations at new sites with comprehensive setup procedures.
Study and Site Management
- Managing subject recruitment and retention: Implementing strategies to attract and maintain participant engagement.
- Executing study protocols: Overseeing daily trial operations to ensure protocol adherence.
- Handling IMP management: Managing investigational medicinal products from storage to dispensation.
- Overseeing PK/blood sample management: Coordinating the collection, analysis, and storage of pharmacokinetic samples.
- Managing laboratories and site files: Ensuring proper laboratory operations and document management.
- Administering data management: Overseeing data collection, storage, and validation.
- Coordinating vendor relationships: Managing interactions and contracts with external vendors.
Quality and Compliance
- Conducting data cleaning: Ensuring data integrity by removing or correcting erroneous data.
- Verifying source data: Confirming the accuracy and completeness of original trial data.
- Analyzing trial data: Interpreting data to provide meaningful insights and identify trends.
- Ensuring compliance: Monitoring and enforcing adherence to clinical trial regulations and standards.
Site Close-Out and Archival
- Reviewing final study reports: Assessing and finalizing study reports based on source documents.
- Closing out sites: Completing all necessary procedures to formally close trial sites.
- Archiving study documents: Safely storing all trial documentation for future reference and compliance.
Our Expertise
- Thorough Monitoring of clinical study on the Right Path with a Risk Based approach.
- Expert in study planning and start up, and throughout study conduct till the close out.
Why Haleus
EXPERTISE-DRIVEN
We’re a specialized CRO with a focus on delivering high-quality clinical trial management and oversight in various therapeutic areas.
Collaborative
Our team approach ensures that we work closely with our clients to meet their needs effectively, leveraging our expertise for their ultimate benefit.
RECOGNIZED EXCELLENCE
Haleus is renowned for its thorough and compliant trial management, recognized within the industry for excellence in clinical research.
Client Focused
We maintain strong partnerships across the healthcare sector, ensuring that our clients achieve the best possible outcomes from their clinical trials.
Our Expertise
RECOGNIZED EXCELLENCE
Haleus is renowned for its thorough and compliant trial management, recognized within the industry for excellence in clinical research.
Haleus Insights Hub
Dive into the latest research, insights, and innovations with our team of experts in the fields that matter most to clinical advancement.
Request For Proposal
We offer an array of niche and full-fledged CRO services, from clinical trial protocol development to post-marketing surveillance. Streamline Your Drug Development with Haleus CRO Expertise