Lotus Clinical Research, Inc. -medical research - clinical trials - inpatient studies - phase I-IV.
Lotus Expertise - high quality inpatient clinical research studies for pharmaceutical and biotech sponsors - evaluation of drugs and devices used in inpatient setting - large database of patient recruitment.
Lotus expertise - hospital based, large inpatient research site with Phase I-IV capabilities.We are a hospital based, large inpatient research site with Phase I-IV capabilities.

Lotus Clinical Research, Inc. conducts high-quality inpatient clinical research studies for pharmaceutical and biotech sponsors, specializing in the evaluation of drugs and devices used in the inpatient setting. Our dedicated patient recruitment team has access to a large database of potential patients and our principal investigators are nationally known in the area of inpatient research.
Specialties - inpatient analgesics - outpatient perioperative analgiesics - bunionectomy - hemorrhoidectomy - hernia repair - anti-emetics - anti-infectives - anticoagulants - PK/PD
When you choose Lotus, you receive the benefit of our expertise in areas such as:

  • Inpatient analgesics
  • Outpatient perioperative analgesics (bunionectomy, hemorrhoidectomy, hernia repair, etc.)
  • Anti-emetics
  • Anti-infectives
  • Anticoagulants
  • PK/PD

With our close attention to detail and high level of personal involvement from the management team and the principal investigators, each protocol is executed in an efficient and timely manner.
Close attention to detail - high level of personal involvement. Management and principal investigators work together to effectively manage each protocol.
Our facility includes a freestanding research unit with Phase I capabilities, 25 rooms/50 beds, -70 freezer, double locked narcotics room.
  • Freestanding research unit with Phase I capabilities
  • 25 rooms/50 beds
  • -70° freezer
  • Double locked narcotics room
learn more
Abstracts with latest information for clinical studies at Lotus Clinical Research. Neil Singla
May 02, 2008 [view here]
A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Parallel-Group, Multiple-Dose Study Of The Efficacy And Safety Of Intravenous Acetaminophen Over 48 Hours For The Treatment Of Postoperative Pain After Gynecologic Surgery.

view all abstracts