Metapharm-cro

YOUR CRO OF CHOICE FOR INFECTIOUS DISEASES

INFECTIOUS DISEASES

MetaPharm Inc. International is an international and independent full-service contract research organization (CRO) known as a reliable and proven partner for many pharma, biotech and medical device companies. We have a great expertise in delivering clinical trials for development programs in the field of infectious diseases. One of our major USPs is our close relationship with sites and a vast network of experts and key opinion leaders worldwide.

LET US BE THE SOLUTION FOR  
YOUR INDIVIDUAL NEEDS

Emphasized by the COVID-19-pandemic, infectious diseases with the potential to severely impact public health and economies have raised high interest for the development of new vaccines and cures. The need for clinical trial expert leadership is paramount to achieve fast bench-to-market timelines, especially when developing new drugs for unmet needs.

MetaPharm Inc. provides this kind of expert leadership across the major markets – EUROPE and USA – that will make the difference for your clinical development programs and for the time to market, making new therapies available even faster for the benefit of public health and economies.

We work with in a network of fully operational local offices across Europe, Russia, Ukraine and the USA. Other areas are covered with well-established partners, all tailored to the need of your project and for the best performance of your trial.

KEY SUCCESS FACTORS IN INFECTIOUS DISEASE STUDY DESIGN & MANAGEMENT

Expertise

Optimal recruitment strategies

Stable & experienced project teams

Telemedicine

Excellent site management & support

Efficiency on time and budget

Consistent high quality

Whether it’s a clinical developmental trial in PHASE I-III, post-authorization study in PHASE IV, study rescue, MetaPharm Inc. has the expertise, know-how and resources to guide you through all phases of development while meeting your objectives and expectations.

INDICATION-SPECIFIC  
EXPERTISE

MetaPharm Inc. International’s team has managed clinical trials (Phase I-IV) for:

  • Human immunodeficiency virus (HIV)
  • Community-acquired Pneumonia (CAP)
  • GI, intra-abdominal infections
  • COVID-19
  • Respiratory virus infection
FROM STUDY DESIGN 
TO STUDY REPORT

MetaPharm Inc.’s full-service portfolio offers you the whole set of fully integrated services while working with one dedicated Project Manager and the PM’s team. You will have the best team for the successful and efficient preparation and setup, submissions, conduct and close-out of your study.

SUCCESSFUL, PRAGMATIC AND  
PROVEN DURING COVID-19

The previous months have shown how dynamic the pandemic situation and the challenges for clinical research can be. With experience, flexibility and a pragmatic approach, MetaPharm Inc. has established new, unique and regulatory sound processes to maintain recruitment in all clinical trials.

KEY FACTORS FOR  
SUCCESS DURING COVID-19
  •  Assessment of local and national pandemic development
  • Identification of ultimate risk factors for patients and study data, prioritization
  • Continuous review and assessment of national latest regulations and requirements
  • Extensive collaboration and communication with national authorities and ethics committees
  • Development of corporate strategy, even prior to official authority regulations and permanent study-specific adaption
  • Supporting sites in implementing preventive measures to ensure patient’s safety when visiting sites for patient visits as well as for CRA onsite monitoring visits and implementing remote ‘site’ visits.