Sponsor/CRO Info

Clinical Research Facility in Miami/Hialeah

Experience, expertise and facility to meet the individual needs of each sponsor and research protocol

The CPMI clinical research facility in Miami location was carefully considered. Our facility was meticulously custom designed and constructed, employing all the knowledge of our experience. We are convinced that our 120 bed research unit is “State of the Art”. We are equipped with the experience, expertise and the research unit facility to meet the individual needs of each sponsor and research protocol. The 24,000 square foot facility is not a hospital, it is not a hotel, it is not an ICU, but it is a custom designed Clinical Pharmacology Research Unit.

Quality & Integrity

CPMI uses a validated environmental monitoring system to ensure the quality and integrity of all pharmacy room temperatures, refrigerated / frozen drugs and samples stored within the CPMI research facility. Security Cameras are stratigically placed throughout our clinical research facility in Miami, both inside and outside, to monitor and record all activity 24 hours a day, 7 days a week. Entry and Exit doors, including fire exits, are alarmed with audible sirens at all times to secure controlled access to and from CPMI. Separation between volunteer inpatient and outpatient areas are strictly secured with locked doors accessible only by staff members with swipe-cards / push-button security codes.
Clinical Pharmacology of Miami is protected by a stand-by 40k watt natural gas generator. In the event of loss of Florida Power & Light power to the building, the strong, but quiet generator automatically detects the loss and starts providing power to all essential portions of the facility. This includes: all the refrigerators, freezers, centrifuges, and security monitoring equipment. The natural gas supply allows the generator to work without interruption for an extended period of time.
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Clinical Studies Conducted
Dr. Lasseter has been Principal Investigator of approximately 1800 clinical studies (over past 40+ years) of the safety and efficacy and mechanisms of action of Phase I, II and III drugs as well as bioavailability and pharmacokinetic studies in normal subjects and in special populations. Numerous clinical studies have been successfully audited by sponsoring institution audit teams and by Food and Drug Administration Audit Teams.
Virtually all studies have been conducted under auspices of active IND applications and approximately 60 successful NDA’s have contained data generated by these studies, including:
  • Acrovastine
  • Aalendronate
  • Amiloride
  • Amrinone
  • Arbutamine
  • Atenolol
  • Benzazepril
  • Candesartan cilexetil
  • Carteolol
  • Caspofungin
  • Ciprofloxacin
  • Dofetilide
  • Enalapril
  • Encainide
  • Eplerenone
  • Recombinant erythropoietin
  • Etodolac
  • Famotidine
  • Felodipine
  • Finasteride
  • Flecanide
  • Fosinopril
  • Galantamine
  • Grepafloxacin
  • Indapamide
  • Irbesartan
  • Leucovorin
  • Lisinopril
  • Losartan
  • Meropenem
  • Milrinone
  • Moexepril
  • Montelukast
  • Nefazodone
  • Nimodipine
  • Nisoldipine
  • Nitroprusside
  • Nizatidine
  • Oxaprozin
  • Penbutalol
  • Pinacidil
  • Piperacillin 
  • Piroxicam
  • Prazosin
  • Ramipril
  • 13-cis retinoic acid
  • Rofecoxib
  • Sinemet CR
  • Sirolimus
  • Sitagliptin
  • Sulindac
  • Tegaserod
  • Timolol
  • Terazocin
  • Tocanide
  • Trandolapril
  • Valsartan
  • Venlafaxin
  • Zafirlukast
  • Zolmitriptan
  • Zolpidem

State-of-the-Art Clinical Research Facility in Miami / Hialeah, FL

  • Screening Department / Interview / Exam Rooms / Prescreening lab & more
  • Out-patient department
  • Secure and monitored PK sample processing laboratory
  • Secure temperature alarm monitored -20 and -70C freezers
  • Secure alarm monitored pharmacy department
  • Secure and monitored CRF / Record rooms
  • Secure Entryways
  • Standby Generator
  • 120 clinical research beds
  • 3 large PK bedded rooms
  • 6 private research rooms (2 plus beds each)
  • 2 very spacious recreational areas for volunteers
  • Supervised Internet access areas for subjects
  • Entire facility monitored by clinical staff, onsite 24 hours a day 7 days a week
  • Security Video Monitor Recording 24 hours a day, 7 days a week
  • Executive suites
  • Conference rooms
  • Record review rooms with monitors’ work areas
  • Study coordinator / offices
  • Women’s health examination areas and ultrasound equipment
  • Data entry / regulatory affairs department
  • Entire facility handicap accessible
  • Spacious private parking
  • QTc Clinical trial ECG monitored research areas equipped with individual telemetry units

Interested in partnering with the ERG network for your next study?

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