Ophthalmic Research Training
9050 Summerfield Rd
Temperance, MI 48182
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(419) 343-7384 |
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| FACT: |
Most Principal Investigators love participating in clinical research, but not the details of day-to-day study mechanisms.
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| FACT: |
Successful Principal Investigators require a team of qualified research personnel, but few know how to design a
team while running a busy practice.
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| FACT: |
Quality Assurance Audits occur everyday, revealing the deficits of not having a qualified team or strong
Standard Operating Procedures in place.
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As a Principal Investigator, signing the FDA Form 1572 or the Investigator Agreement establishes YOU are taking
full responsibility for complete management of the clinical research study and procedures at your site. But...
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Are you new to Clinical Research? Or are you taking steps to expand your research practice?
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Do you have strong Clinical Research Standard Operating Procedures in place?
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Are you certain your staff follows Good Clinical Practices in research?
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Do you have a qualified team in place with documentation of training?
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Does your team report to you on a regular basis so that you are constantly aware of everything that is
occurring, as it happens?
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Do you scrutinize protocols and budgets to make sure it's a good situation for your research practice development?
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Do you understand the requirements of the Regulatory Binders?
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Do you have strategies in place that will help your recruitment efforts?
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Are you prepared so that site qualification or site initiation visits will have a positive outcome?
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Do you know the repercussions of not monitoring the Monitor?
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Will you survive a Quality Assurance Audit?
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Ophthalmic Research Training Services comprehends these situations and provides the training, tools and support
required to be highly successful in your research practice in a variety of formats.
Get started on the right Ophthalmic Research Training plan today. It's so easy, just email or call me for a free confidential consultation of
your research needs.
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