SpinoS BA/BE division has an experienced scientists comprised of, Clinical pharmacologists and life science personnel.

SpinoS team has an experience of conducting more than 300 studies together which results in delivering quality job.

Successfully faced two USFDA audit with NIL 483.

We have conducted over 300 studies with a back up of 30,000 healthy subjects including Post menopausal females.

We have expertise in conducting

  • Single & multiple dose studies
  • Fasting & Fed studies
  • Food Effect studies
  • PK PD studies
  • Cross over and parallel studies
  • Replicate studies
  • Proof of concept studies
  • Special population studies (postmenopausal & adult female studies and geriatric studies)

BA/BE studies are conducted in SpinoS are in extremely controlled environment and all activities are strictly driven through SOPs.

We are expertise in delivering the project on time with a turn around time of 45 days from the initiation till the final report.

The studies conducted are approved by the Independent ethical committee, all the procedures in clinical and bioanalytical are SOPs driven, in accordance with current GCP, GLP standards and applicable regulatory requirements.

Individual project managers will be allotted to each project and close coordination with sponsor to cater all their requirements.

With a vision of most preferred research partner we believe in developing cordial relationship with our entire sponsors through exclusive and efficient project management to all their projects.