Clinical Management and Development

We are Working Very Hard To Ensure That Your Clinical Trials From phase II to IV Runs In Time and With The Follow Of The GCP ICH Guidelines. We Offer You Improvement In Clinical Development Of Niche Treatments, Blockbuster Drugs, And Biosimilars Always Following Our Main Thinking To Helping Save Lives.

Clinical Research And Development Is Very Complex. Let Us Become The Right Partner To You Making Your Path Easier. We Work Hand-in-Hand With Our Sponsors Because We Know The Importance Of Every Contribution They Could Bring To People. From This We Develop Strategic, Flexible Approaches That Leverage Clinical Informatics And The Latest Technologies In Clinical Management To Maximize Safety And Efficiency Taking Data-Driven Decisions For Every Study, Optimizing The Data Integrity For The Sponsor.  Our Functional And Therapeutic Expertise Spans A Broad Range Of Indications, Including Cardio-Metabolic, Gastrointestinals, Oncology/Hematology, Infectious Diseases, Neurology/Psychiatry and Endocrinology Diseases.

What You Can Expect

You Get A Single Point Of Contact, Expertise In CDS Services, And Accountability And Transparency With A Proven Track Record Of Successful Delivery. Timelines And Risks Are Managed Proactively, Applying Knowledge From Past Experiences To Ensure Accurate Financial Management.

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Let Our CRAs Take Care of Your Clinical Research Monitoring

Our Dedicated Clinical
Research Associates And CRAs And CTAs Monitor Studies Worldwide. Each CRA Focuses By Far On Two Therapeutic  Areas, So They Have Deep Knowledge Of The Patients, Investigative Sites And Specific Challenges Involved. All Clinical Trial Monitoring Team Members Receive Ongoing Training To Ensure They Are Completely Up-to-Date With Current Legislation, Techniques And Technologies. They Are Supported By Our Central Monitoring Groups.

Optimazing Studies Reducing Risk And Saving Money

Today, Drug Developers Face An Increasingly Complex And Evolving Landscape. Regulatory Agencies Are Demanding Smarter, More Efficient Risk-Based Methodologies To Improve Data Quality. In Addition, The Increasing Cost Of Research And Adoption Of EDC Technologies That Provide Real-Time Access To Data Have Forced The Industry To Look At Optimized Methods Of Conducting Clinical Studies. By Employing a Risk-Based-Monitoring (RBM) approach, We Can Holistically Evaluate Each Individual Study And Determine The Right Organizational Structure To Support Both Central And On-site Monitoring And See Data Trends In Real-Time.

Providing Specialist, Technology-Enabled TMF Solutions and Support

Clinical Trials Can Be Large And Complex, Involving Many Departments And Partners. As A Result, Trial Master File (TMF) Management Can Become A Difficult Task. We Are A Specialist Provider Of Technology-Enabled TMF Solutions And Other Support Services For All Our Clinical Research Market.