Clinical Trial Pollen/Mold Measurement
When data is submitted to the FDA for an allergy or asthma
clinical trial, it must be complete and accurate, with no
unknowns. Sponsors and investigators rely on calibrated, well-maintained
medical equipment, standardized allergen extracts
and accurate patient data to prove the safety, efficacy or new
indication of their drug. Because of varying quality of pollen
counts available to the public, more researchers are turning
to SDI to ensure that pollen data for their clinical trial is as
accurate and well documented as possible.
For over ten years, SDI has worked with large pharmaceutical
companies, CROs and individual investigator sites to provide
them with pollen counting services. We are able to provide
every customer with a variety of different services to fit their
protocol. Among these services, we offer:
- Consultation for placing investigator sites and initiating
study start dates.
- Calibrated Rotorod samplers for individual
investigator sites.
- Analyzing of pollen and mold samples from one central,
accredited laboratory and complete pollen count reports.
- Final, well organized databases of pollen and mold counts,
with complete documentation.
- Audit ready, comprehensive pollen and mold counts
to strengthen your submissions to the FDA.
With our services, you will be assured pollen and mold
measurements that are accurate: samples taken by calibrated,
well-maintained sampling equipment, analyzed by one central,
certified laboratory, and organized into datasets that easily
fit into your protocol. For more information on how we can
provide your clinical trial with pollen and mold counts.
For more information, please contact us.
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