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About Us

At AIM Clinical Research, we are dedicated to advancing clinical research through our experienced global team of industry experts. Our focus on cost efficiency allows us to provide high-quality, tailored solutions that deliver exceptional value without compromising on service. We understand the critical importance of timely results, and our qualified workforce is committed to meeting deadlines consistently. Transparent communication is at the heart of our client relationships, ensuring you are informed every step of the way. Regular KPI reports provide valuable insights into project progress, enabling effective resource management.

We are not just a service provider; we are your partners in innovation and growth. Utilizing industry best practices such as Lean Six Sigma and ISPE GAMP Risk-Based approaches, we enhance the quality and efficiency of our services while proactively identifying and mitigating risks. Our mission is to empower your research efforts with customized solutions that drive success and advance the field of healthcare.

Together, we can shape the future of clinical research, ensuring that your projects contribute to meaningful advancements in patient care.

Quality Standards Delivered

At AIM we prioritize the highest quality standards to ensure the integrity and reliability of our clinical research services. Our commitment to excellence is reflected in our adherence to industry regulations and best practices:

  • Compliance
  • Continuous Training
  • Quality Assurance

Our Team

Our global team of 16 professionals brings together diverse expertise to drive innovation in clinical research. Comprising Directors, ClinicalMedical Professionals, Data Management / Statistical team our multidisciplinary team is dedicated to delivering exceptional results for our clients. Each member is selected for their unique skills and experience, ensuring a comprehensive approach to every project:

  • Leadership
  • Technical Expertise
  • Clinical Insight
  • Commitment to Excellence

Client Satisfaction

At AIM, client satisfaction is at the heart of our mission. We prioritize building strong, collaborative relationships and delivering exceptional results.

Here is how we ensure your needs are met:

  • Personalized Approach
  • Transparent Communication
  • Timely Delivery
  • Ongoing Support

Quality Standards Delivered

At AIM we prioritize the highest quality standards to ensure the integrity and reliability of our clinical research services. Our commitment to excellence is reflected in our adherence to industry regulations and best practices:

  • Compliance
  • Continuous Training
  • Quality Assurance

Our Team

Our global team of 16 professionals brings together diverse expertise to drive innovation in clinical research. Comprising Directors, ClinicalMedical Professionals, Data Management / Statistical team our multidisciplinary team is dedicated to delivering exceptional results for our clients. Each member is selected for their unique skills and experience, ensuring a comprehensive approach to every project:

  • Leadership
  • Technical Expertise
  • Clinical Insight
  • Commitment to Excellence

Client Satisfaction

At AIM, client satisfaction is at the heart of our mission. We prioritize building strong, collaborative relationships and delivering exceptional results.

Here is how we ensure your needs are met:

  • Personalized Approach
  • Transparent Communication
  • Timely Delivery
  • Ongoing Support

Professionalism

  • Your trust is our greatest asset, and we pledge to treat you with the integrity and respect that reflect our commitment to your success.
  • At our core, we believe in treating every client with the respect and integrity that their trust deserves, ensuring a seamless and collaborative experience.
  • Your partnership is invaluable to us, and we are devoted to upholding the highest standards of integrity and courtesy in all our interactions.

Core Services

At AIM, we offer a comprehensive suite of clinical research services designed to support your projects from inception to completion. Our expertise spans multiple phases and therapeutic areas, ensuring that you receive high-quality, reliable results.

Here's a brief overview of our key services:

End to End Clinical Trial Services (Phase I to Phase IV)

Our End-to-End Clinical Trial Services provide comprehensive support from initiation to final reporting, Industries we cover

  • Pharmaceutical
  • Nutraceutical
  • Cosmetics
  • Herbal and Ayurvedic
  • Food Supplements
  • Nutritional and Dietary supplements
  • Medical Device

Regulatory Services

  • Global Regulatory Compliance –FDA/ EMA/ ANVISA/ DCGI/21 CFR part 11/820, PMDA, Health Canada, GxP, ISO
  • Regulatory Dossier Compilation
  • SEC Meeting and Expert Management
  • Regulatory approvals for Phase I-IV, device studies and BE studies
  • Safety Reporting

Quality Assurance Services

  • Qualifications of GCP/ GLP/ GMP/ PV/ ITQA audit compliance
  • Computer System qualifications: CSV/ CSA Risk based compliance
  • Process: GAP Analysis and Risk mitigation

Clinical Trial Key Services

Our Clinical Trial Key Services streamline the research process, ensuring efficient study design, regulatory compliance, and data management. We provide comprehensive support from planning to execution, helping you accelerate the path to successful outcomes.

Heres a brief overview of our key services:

Medical Writing

Our Medical Writing services deliver clear, precise documentation that meets regulatory standards along with ICH E3 compliance and effectively communicates complex clinical data.

  • Protocol Preparation and finalization
  • Informed consent form Preparation and finalization
  • Patient Diary/ Subject diary Preparation and finalization
  • Clinical Study report Preparation and finalization
  • Pharmacokinetic analysis plan
  • CRF Preparation and finalization
  • Study Design and Protocol Development- Patient based BA-BE studies

Clinical Data Management & Biostatistics

  • Data capturing, cleaning, reconciliation and review
  • Generate Tables, Listing and Figures for Data Analysis
  • Sample size calculation and statistical inputs to protocol for study results analysis.
  • Database Design and Data Management
  • SAPs development and planning
  • SAE reconciliation
  • Electronic Data Integration and Statistical Report preparation
  • Develop the case report form (eCRF)
  • Customized CRF design, verification and Validation
  • SAPs development and planning

Clinical Operations

  • Subject Recruitment and screening
  • Site Management
  • IMP management
  • Medical Monitoring and Safety Management
  • Regulatory and IEC/ IRB submission
  • Site Selection, initiation, monitoring and closeout
  • Vendor Management

Past work

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Contact Us

AIM CLINICAL RESEARCH PVT LTD

301 & 302, Swami Narayan Business Park,Opp, Swami Narayan Plaza-I,
Opp, Gokulesh petrol Pump Narol Circle Narol Ahmedabad INDIA