Our Services

At ZEED Pharmaceutical Solutions, we offer comprehensive and customized solutions for every stage of pharmaceutical and medical device development. Our team of experts, with deep knowledge of national regulations and Good Clinical Practices (GCP), supports our clients from strategic planning through the execution and monitoring of their studies.

We ensure quality, regulatory compliance, and efficiency in every process, optimizing time and resources so that your projects achieve reliable results ready to support the safety and efficacy of your products in the Mexican market.

1. Planning and Management of Clinical Research Projects

For the planning and development of your research, we offer our clients the following services:

Design and Development of Clinical Research Protocols in all phases: preclinical and clinical Phases I–IV, including chart reviews
Investigator Engagement
Research Human Resources
Site Selection
Training for Investigators and Site Staff
Training Tools
Randomization
Working and Follow-up Meetings
Preparation of Submission Packages for Ethics Committees, Institutional Review Boards (IRB), and COFEPRIS

3. Scientific Writing

Its main characteristic is clarity in conveying the client’s ideas to different audiences, with the goal of achieving effective communication.
Writing of:

Protocols
Investigator’s Brochure
Patient Information
Physician Brochures
Medical Reports
Prescribing Information (PI)
Scientific Articles
Conference Posters
Final Study Reports

5. Pharmacoeconomics

The development of new therapeutic strategies brings the potential for more effective treatments, although the costs involved are usually higher. Pharmacoeconomic analyses allow the advantages and disadvantages of new therapies to be evaluated in relation to their costs, providing valuable information that can be used in negotiations with relevant regulatory and healthcare authorities.

Cost-Minimization Studies
Cost-Benefit Analysis
Cost-Effectiveness Analysis
Cost-Utility Analysis

7. Training

We offer courses in the following areas:

Good Clinical Practices (GCP)
Monitoring
Clinical Research Regulation in Mexico, USA, and EU
Pharmacoeconomics
Biostatistics
Pharmacokinetics

2. Execution and Development of Clinical Research Studies

During the development of research studies, we provide the following services:

Project Development in any phase: preclinical and clinical Phases I–IV, including chart reviews
Investigator Preparation and Evaluation
Site Training
Recruitment Strategies
Initiation visits, BA/BE monitoring, Phase II–IV monitoring, and close-out.
Monitoring
Audits
Ensuring Compliance with ICH-GCP
Quality and Safety Reports
Follow-up Reports
Drug Accountability
Adverse Event Collection and Reporting

4. Biostatistics

One of the challenges faced by healthcare professionals is having the analytical tools necessary to make proper use of the available information for decision-making in this sector. To address this, we offer our clients the following services:

Database Design
Statistical Analysis Plan
CRF Design (Case Report Form)
Database Analysis
Data Entry
Data Validation
Statistical Modeling

6. Scientific Translation

Thanks to our experienced translators, extensively trained in their respective fields, our scientific translation services deliver superior quality. We provide both straightforward translations and translations certified by a sworn translator.

English
Spanish
French
Portuguese
German