Company Profile

Sourcing Inquiry Logo Parexel Consulting

Parexel Consulting

Regions
Europe, North America, …
Regions
Europe, North America, South America, Asia, Australia & New Zealand
Countries
Mexico, Germany, …
Countries
Mexico, Germany, United Kingdom, United States
Size
1000+
Specialty
Human Medicines, Biopharmaceuticals, …
Specialty
Human Medicines, Biopharmaceuticals, Generics, Cosmeceuticals, Medical Devices
Service category
Regulatory services - CMC writing - medical writing
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Result

Average value of all company ratings [2]

Criteria

  • Expertise / Capability 4.5
  • Price-Performance Ratio 3.5
  • Confidentiality 5.0
  • Timeliness 4.0
  • Flexibility 3.5
  • Quality of work 4.0
  • Project contacts and care 4.0
  • Geographic proximity 3.5
  • Culture fit 4.0
  • Environmental sustainability ---
  • Financial stability ---
  • Contract / invoice performance 3.0

Single ratings

"Good mix of regulatory experience"

Projects

Orphan drug application for a biological

Pro and contra

  • Good mix of regulatory experience, clinical understanding and practical competence. Very good medical writers with indepth experience in orphan drug submissions. Successful outcome-fast process and almost no questions.

  • no comment

good

Criteria

Expertise / Capability
4.0
Price-Performance Ratio
3.0
Confidentiality
5.0
Timeliness
4.0
Flexibility
3.0
Quality of work
4.0
View all »

[Verified Buyer from Germany]

"A real one-stop-shop"

Projects

Parexel helped us with a global regulatory submission, first with FDA, then with EMA

Pro and contra

  • The company's capabilities, the broad range of services and expertise over a large variety of products is obvious. They have done a great job in timely preparing the NDA first and then to update the dossier for the MAA submission. Great knowledge, skills and team.

  • no comment

good

Criteria

Expertise / Capability
5.0
Price-Performance Ratio
4.0
Confidentiality
5.0
Timeliness
4.0
Flexibility
4.0
Quality of work
4.0
View all »

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