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Clinical research trial support by DDA Medical
gives medical device manufacturers, regardless size, the resources they
need to conduct large-scale clinical trials with maximum process and
cost efficiency.
DDA Medical’s clinical research trial (CRT)
support provides medical device manufacturers with the management software,
database programming, and supportive technology necessary for completing
clinical trials and the approval processes with efficiency. A streamlined,
organized clinical trial process helps make advanced medical devices
available to the patients who need them most. DDA Medical builds the
clinical trial management systems, software, databases, and programs
that give medical device manufacturers online tools that can track patients,
archive documents, store data and analysis for results, create secure
Intranet portals, and more.
DDA Medical strives to provide medical device
manufacturers, government or privately-funded research institutes, contract
research organizations, and more with the tools that lead to an efficient
clinical trial and approval process.
DDA Medical Tools
for Clinical Trial Patient
and Investigator Recruitment
Medical device manufacturers who conduct clinical trials require both
patients and investigators. Manufacturers who are in Phase 1 of a clinical
trial may find recruitment simple. However, manufacturers who are conducting
large scale Phase III trials require much larger numbers. DDA Medical
designs medical websites and medical print advertisements that reach
out and inform patients and their healthcare providers about your clinical
trial. This type of information can start important conversations between
patients and healthcare professionals. Within CRT medical websites,
you also can archive approval forms which are readily available to both
patients and doctors.
Worldwide Support
for Clinical Trials
Conducted in Multiple Locations
If your clinical trials are in Phases I and II, you are probably conducting
them within a localized area. If your clinical trials are in Phases
III or IV, however, you may be conducting large-scale studies out of
several centers across the country or even around the world. DDA Medical
provides the referral and recruitment support services that help you
locate the investigators and other medical professionals who will conduct
a trial then collect the resulting data in their center. By having DDA
Medical construct online portals that feature a secure Intranet, you
can organize the data collection process, facilitate instantaneous communication,
and review results from geographic locations thousands of miles apart.
Archiving and
Retrieving Documents
for Clinical Trials
Clinical trials are a highly regulated process which must comply with
the standards of the FDA as well as Institutional Review Boards (IRB).
By designing and developing medical website portals, DDA Medical allows
you to upload documents such as investigators’ credentials and
eligibilities, trial protocols, patient recruitment materials, Informed
Consent forms, statistics, data sheets, and more. DDA Medical clinical
trial support makes obtaining approval and analyzing results efficient
and cost effective.
Phase III Clinical
Trial Support Tools
Establishing how a procedure involving a new medical device affects
a patient’s daily life through complications and side effects
is an important aspect of the Phase III clinical trials. DDA Medical
builds online and electronic patient diaries that can be filled out
and submitted through Intranet or Internet portals. Results from patient
diaries are easily recorded by clinical investigators.
Post-Marketing
Surveillance Tools
for Clinical Trial Phase IV
By the time medical device manufacturers conduct Phase IV clinical trials,
their device has been approved by the FDA. Now, manufacturers may need
to record long terms results in a larger patient population, or they
may need to perform studies for other possible uses of the medical device.
DDA Medical tools simplify the post-marketing surveillance process.
Medical device manufacturers can reach patients through specially-designed
Intranet websites, while other online recording devices can make results
immediately available for investigator analysis or meta-analysis.
Meta-Analysis
and Overview Support
If a medical device manufacturer is interested in clinical trial overviews
or meta-analysis support, DDA Medical provides the communication tools
that market and promote your cause. From medical CD-ROMs and DVDs to
medical print media such as direct mailings or patient brochures, customized
outreach tools by DDA Medical targets the other organizations who are
conducting similar clinical trials.
DDA Medical is a division of Dynamic Digital Advertising
and has the experiences, skills, and in-house staff necessary for building
whatever is required for more efficient and more effective clinical
trials. Based in the greater Philadelphia area in Bucks County, Pennsylvania,
DDA’s regional list of clients includes those from states such
as New York, New Jersey, Delaware, and Maryland as well as Washington
D.C. and the rest of the United States.
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