MDBlackBox available free to physicians, clinics and patients was founded by a hospitalist doctor who was not satisfied with available EMR systems sufficiently eased challenges while simultaneously providing safe, secure and user-friendly access for patients.

The user friendly MDBlackBox is not only for patient record keeping, but also appointment scheduling, billing, laboratory and radiology order entry, electronic prescription transmission, staff management, and arrangement of referrals yet is designed to be user-friendly, secure and easily used from any web-accessible computer, phone, or tablet.

MDBlackBox securely and reliably uses the same security standards used by online banking systems. Keeping all of a patient’s records in a  reliable data vault prevents information gaps that can develop when a patient sees multiple practitioners.

MDBlackBox is a SaaS (Software as a Service) product designed for practices ranging from solo practitioners to large multi-facility clinics. Its wide spectrum of features is robust but designed to be user-friendly, bring the gap together of communicating with patients, manage their care and follow their progress as well as substantially increase practice management efficiency and aid in human resource management and practice marketing.

The wellness tools help patients monitor and relay their daily condition and activities improving compliance with ongoing treatment programs such as weight management or mobile device text reminders to help patients maintain their medication schedules.

As the nationwide goal of universal EMR adoption by 2015 approaches, MDBlackBox is an excellent across-the-board solution that is ready right now.  Interested physicians and clinics can start the process of evaluating and adopting MDBlackBox with a visit to www.mdblackbox.com.

About MDBlackBox

MDBlackBox addresses the complexities and critical needs of today’s healthcare environments by providing a revolutionary web-based, on-demand platform for record keeping and patient support that reduces the costs and challenges associated with licensing, implementation, integration and support usually experienced with leading enterprise software solutions. With MDBlackBox providers can deliver the highest level of care and service to their patients simply, easily and inexpensively. Learn more at www.mdblackbox.com.

Gather feedback and market research from them in discussion forums, surveys, and private messaging. Give online incentives and rewards for employee engagement and loyalty.

Launch incentive programs for doctors and nurses who provide your medication to their patients. Announce luncheons, WebExes, and conferences. Keep track of attendance with Calendar and Events!

Example Solution:

• In Depth Data Collection

A pharmaceutical company wanted to create a community of medical professionals that used their medication to keep them informed of side effects, current research, conferences and incentives. With Trunity Connect they were able to invite all of their clients, facilitate discussion between doctors as to treatment methods and solutions to disease, and further research by gathering real-life use cases and success stories. The same medical professionals were inspired to join one of their annual conferences that was announced on the portal, making it one of their most successfully attended to-date.

For more information visit http://www.trunity.com

The FDA has ramped up surveillance and we have seen an increase in the number of warning letters issued to manufacturers. We have seen a corresponding increase in GMP upgrade projects in the industry.

This workshop will provide the audience with information to perform a gap analysis of their existing GMP systems by reviewing the major areas of concern listed by FDA inspectors. The systems covered will include FDA requirements for OOS Investigations, Pharmaceutical and Biologics Stability Programs and Method Validation.

This workshop will provide the audience with an overview of the key systems which have been mentioned by FDA Inspectors as major areas of concern in FDA Regulated Pharma Laboratories. During the discussion of each of the areas listed below, the Workshop participants will work through a series of related FDA 483s to fully understand FDA expectations and the errors which lead to the 483s.

Hurry. Register early because space is limited. Your tuition fee of $599 includes the workshop, all course materials and lunch.

Location:
Hampton Inn Philadelphia-International Airport
8600 Bartram Ave
Philadelphia, Pennsylvania
USA 19153

Areas Covered:

1. FDA requirements for OOS Investigations

• Phases of an Investigation
• CAPAs, Investigation Conclusion and Documentation of the Investigation
• 483s related to OOS investigations and lessons learned from them

2. FDA requirements for Pharmaceutical and Biologics Stability Programs

• Overview of ICH and WHO requirements for Stability Programs
• Stability study requirements for Phase I, Phase II and Phase III clinical studies
• Stability methods and specifications
• 483s related to Stability Programs and lessons learned

3. FDA requirements for method validation

• Overview of relevant ICH guidances and USP <1226>
• Requirements for different method types
• 483s related to method validation and lessons learned

Course Schedule:

The course schedule is provided below. Each session will include a 10 min break.

8.30-9 AM: Introduction and overview of the GMPs.

9-11 AM: Out of Specification Investigations. Includes a 30 minute hands-on interactive exercise

12-1 PM: Lunch

1-3 PM: Stability. Includes review of relevant recent 483s in an interactive exercise

3-5 PM: Method Validation. Includes review of relevant recent 483s in an interactive exercise

Bonus Material:

Each attendee will receive a CD with the relevant regulatory and guidance documents.

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