iMEDGlobal  
 
   
 
 
   
Focussed Service
   
   
iMEDGlobal is uniquely focused in providing comprehensive turn-key regulatory compliance services to augment any drug safety, regulatory, clinical and R&D department.

To know more about our capabilities
click here
 
     
 
     
Spacer
 
Technology
 
  Technology

Identify Deliver & Secure Value


iMEDGlobal’s Consulting approach is more than giving advice. Our consultants not only focus on recommendations, but assists in building consensus and commitment to improve organizational effectiveness.
 
     
     
vutton
 
   
   
   
iMEDGlobal is uniquely focused in providing comprehensive turn-key regulatory compliance services to augment any drug safety, regulatory, clinical and R&D department.

To know more about our capabilities
click here
 
       
     
Spacer
 
Regulatory Affairs
 
  Regulatory Affairs
Regulatory Submission process is a critical activity and is bound by various dimensions that have to be efficiently addressed:
 
     
     
vutton
 
   
   
   
iMEDGlobal is uniquely focused in providing comprehensive turn-key regulatory compliance services to augment any drug safety, regulatory, clinical and R&D department.

To know more about our capabilities
click here
 
       
     
Spacer
 
Pharmacovigilance
 
  Pharmacovigilance
Individual case reporting with on time, high-quality, consistent data capture and management practices is the hallmark of an exceptional Pharmacovigilance services provider.
 
     
     
vutton
 
   
   
   
iMEDGlobal is uniquely focused in providing comprehensive turn-key regulatory compliance services to augment any drug safety, regulatory, clinical and R&D department.

To know more about our capabilities
click here
 
       
     
Spacer
 
Clinical
 
  Clinical
iMEDGlobal provides clinical trial monitoring and project management solution maintaining the highest standards of ethics, quality and confidentiality.
 
     
     
vutton
 
   
   
   
iMEDGlobal is uniquely focused in providing comprehensive turn-key regulatory compliance services to augment any drug safety, regulatory, clinical and R&D department.

To know more about our capabilities
click here
 
       
     
Spacer
 
Reformulation
 
  iMED-RE
iMED-RE includes all the requirements for reformulation including, global project management, toxicology, safety trials, efficacy trials, clinical operations, clinical data management, regulatory affairs, medical affairs, and claims management.
 
     
     
vutton
 
   
   
   
iMEDGlobal is uniquely focused in providing comprehensive turn-key regulatory compliance services to augment any drug safety, regulatory, clinical and R&D department.

To know more about our capabilities
click here
 
       
     
Spacer
 
Success Story
 
  iMedGlobal Succcess Story
iMEDGlobal designed and built a data extraction layer which interfaced with the regional consumer response systems to compile and consolidate cases from their respective regions.
 
     
     
vutton
 
       
 
Process Consulting
   
 
Process Consulting
 


Identify Deliver & Secure Value


iMEDGlobal’s Consulting approach is more than giving advice. Our consultants not only focus on recommendations, but assists in building consensus and commitment to improve organizational effectiveness. Our consulting assignments not only generate cost savings, but the real advantages are improved turn-around times and increased quality and regulatory compliance.


 
       
 
 
 
My iMED

“Happy minds yield Great Solutions and Services”.


We strive to make iMEDGlobal a place where people come not just to work, but to enjoy what they like the most! It provides an ecosystem for entrepreneurs to push their limits and young enthusiasts to burgeon as future leaders.

 
 

divider-line
 
 
News & Events

October 2014


Dittas Formoso, Vice President, Business Development, APAC region for iMEDGlobal will be speaking at the 3rd General Membership Meeting of the Philippine Chamber of Pharmaceutical Industry on October 28. Ms. Formoso will host an interactive discussion, “How Emerging Markets are Driving the Transformation of the Pharmaceutical Industry.” The meeting will be held from noon to 3:00 pm in the Columbus Room of Discovery Suites in the Ortigas Business Center, Pasig City.