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The Implant Technology Research & Development team is dedicated to providing progressive formulations to our Licensees to ensure the finest quality, consistent products in pharmaceutical implant technology. Our trade secrets have allowed us to design and test products that exceed dissolution expectations. Yielding less drug usage over time, fewer pellet insertions in some patients, and increased patient compliance.
With an eye on the future, Implant Technology aspires to provide leading innovative patient care solutions. Our efforts are strongly focused on the research of new product formulations, devices and protocols identifying better patient outcomes in markets such as drug addiction, fertility, cardiovascular disease and hormone replacement therapy.
Our Research & Development team, using primary research investigations, will work with you in the development of new pellet formulations to address the specific needs of your patients. Consult with our pharmacy specialists to design unique compounds to target serious health challenges. Any medication that can be delivered intravenously, intramuscularly, intradermally, or subcutaneously has the potential for a pellet implant application. Imagine the potential for delivering consistently dosed medications or nutrients without the concerns of compliance or abuse.
Our team has compiled a library of standard operating procedures based upon our regulatory compliant laboratory and pharmaceutical order processes developed for delivering patient specific sterile product orders. Your pharmacy will receive manuals and professional training opportunities to implement all necessary step to setting up and operating your pellet implant facility.
Implant Technology is committed to delivering the best equipment, supplies, and expertise to meet the needs of our Licensees. Through research and development, we endeavor to stay on the cutting edge of pellet implant technology, continually delivering resources and training to our Licensees.
The chain of command is provided and implemented by our dedicated pharmacists and quality control staff to ensure that every pellet compounded passes our extensive testing process to ensure sterilization and potency and uniformity. All batches go through a vigorous requirement to meet all compliance needs and personnel take part in these roles to ensure quality and safety.
Our custom made implant pellet process specifies compliance practices to USP-797 and ISO-Class 5 clean room regulations, exceeding the standards required for sterilization and quality.
Our resources provide for non-bias testing from independently registered FDA testing labs to promise sterility and potency with each and every batch made available using our custom, cloud-based CRM application.
All batches must go through dissolution test associated with day-to-day validation testing on any device that may affect the sterility of the final product. Also 3rd party testing for an analytical testing facility is required at different intervals, to validate the process.
A standard operating procedure has been developed and is implemented by our Compliance Department to ensure that the Implant Technology Licensees adopt the full process as part of their internal QA/QC.
Implant Technology is supported by a highly regarded team of medical experts. Our Medical Quality Board is comprised of a diverse group of medical professionals: Pharmacologists, Anatomist, Physicians, Pharmacists, Agriculturalists, Microbiologists and others.
The purpose of our Medical Quality Board is to provide insight regarding the constantly evolving medical industry and the best practices for achieving revolutionary patient outcomes. Through the means of medical research and development, improved regulation modalities, integrative medicine solutions, testing and analytics, technology innovations and new visionary systems, Implant Technology will meet and exceed the needs of our clients and patients.
In the last decade, desire for customized therapeutics and medically and esthetically enhancing custom products drove the medical industry in a new direction. A market demand was created for an array of wellness products and services.
In America, the Alternative Medicine market has quickly grown to a $34 BILLION per year industry.
The Pellet Implant Technology System presented to you by Implant Technology is designed to allow you to easily enter this dynamic field, presenting the opportunity to improve patient care, as well as your financial goals. The plan is customizable to fit with your current business practices, giving you the opportunity for an additional revenue stream, greater patient population, and new market access.
With your investment and the expertise of our dedicated team, you will be afforded a tremendous opportunity to enter into a new realm of treatment modalities and truly engage your physicians with real therapeutic solutions for a patient community who are desperately in need.
The Implant Technology pellet production protocol allows pharmacies to quickly and easily integrate pellet therapy into their current workflow, and to offer more affordable pricing for medication therapy than would be allowed with many conventional pharmaceuticals. In most cases hormone implants can last between 3 and 6 months, therefore, in comparison to traditional pharmaceutical prescriptions, the patient cost of pellet therapy can be very cost effective and convenient.
The pellet implant technology system presented to you is designed to allow you to easily dive into this dynamic process, allowing you the opportunity to improve patient care, as well as your financial goals. The plan is customizable to fit with your current business practices, giving you the opportunity for an additional revenue stream, greater patient population, and new market access. Align your practice with Implant Technology and discover a new world of opportunities in outcome-based medicine.