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| Articles by John Robinson |
51. Handle internal investigations thoroughly, else employees could approach law agencies
September 23, 2016
Employees have a right to approach external sources such as the Equal Employment Opportunity Commission (EEOC), the National Labor Relations Board (NLRB), Wage and Hour, private attorneys, and juries against the employers, when feel that their legitimate complaints are not being heard by their emplo...
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52. Maximizing profits and patient outcomes during times of dwindling reimbursements
September 22, 2016
Shrinking professional services reimbursements from all insurance companies is a fact that all practices are facing. With patient footfalls falling and operating costs skyrocketing; there is a need for everyone to look at ways by which to generate additional revenue opportunities with their existing...
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53. Medical products need to be validated for Radiation Sterilization
September 21, 2016
“Do it right the first time” should be the mantra for medical device manufacturers that plan to make radiation products. Choosing the most functional and radiation resistant materials for their medical device will help them avoid the trouble of going through the post launch cycle of product revision...
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54. Ensuring compliance with healthcare laws is of utmost importance for healthcare providers
September 20, 2016
Compliance with the many laws, as well as implementation of the necessary compliance initiatives are the means by which healthcare providers and entities or organizations involved in any type of healthcare transaction, especially those who bill or are involved with services payable by a CMS program,...
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55. Cleaning validation should have a policy designed to meet harsh regulatory requirements and princip
September 19, 2016
Compliance with the required cleaning validation regulatory compliance guidelines set out by the regulatory authorities such as the FDA, WHO, PIC/S and EU is essential for those who work in facilities which involve cleaning. The reason for which adherence to these regulatory guidelines is necessary...
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56. Implementing the 510 (K) correctly in compliance with the latest proposed FDA changes
September 16, 2016
A 510(K) is a premarket submission made to FDA to demonstrate that a device to be marketed is at least as safe and effective, meaning that which is substantially equivalent, to a legally marketed device that is not subject to premarket approval (PMA). There are three types of Premarket Notification...
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57. Applied Statistics for product and process evaluation in design and manufacturing
September 14, 2016
Evaluating product and processes is an imperative for almost all design and/or manufacturing companies. These are the reasons for which this evaluation needs to be made: o Managing risks o Validation of processes o Establishing product/process specifications to QC to such specifications o Monit...
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58. The ISO 13485:2016 standard is new and needs to be looked at afresh
September 13, 2016
With the ISO making the final version of the ISO 13485:2016 standard available; it is now up to companies to start planning ways of implementing it. The major area in which it differs from the earlier version (of 2003) is in the extent of its alignment with the FDA’s Quality Management System (QMS) ...
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59. GlobalCompliancePanel's onsite trainings serve the exact learning needs of regulatory compliance pr
August 21, 2016
Professional trainings come with their own set of distinct advantages. When they are offered in the form of in person, live conferences; they get the Expert to come down to a fixed venue and get to learn from the expert. However, this medium does not address all the problems that professionals usual...
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60. Event Manager
June 09, 2016
Opportunity to Advertise with GlobalCompliancePanel
GlobalCompliancePanel presents a fine opportunity for getting businesses to advertise their products and services on its website. Businesses can now place their ads on the GlobalCompliancePanel website, http://www.globalcompliancepanel.com/...
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Author: John Robinson
