RPH SERVICES

TRAINING AND QUALIFICATION

RPH group has 19 years of experience in the Latin American business for Nuclear Medicine and counts on highly skilled specialized professionals. All this know-how is available to the market, with trainings in the fields of Hospital Radiopharmacy, PET and industrial, promoting new technologies, implementing Good Manufacturing Practices and adjustment of Nuclear Medicine Services according to the prevailing legislation.

THE MODALITIES OF TRAINING AND QUALIFICATION ARE:

  • Quality Control
  • Good Manufacturing Practices in Radiopharmacy

OUTSOURCING PROGRAMS

The objective is to offer a complete solution to radiopharmacies, assisting with the planning and the accomplishment of improvements, adjustment of the prevailing legislation, quality assurance, cost optimization, insertion of new technologies and protocols and development of clinical trials and innovations. With a minimum duration of 12 months, the program is comprised of four stages:

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    Stage 1 – Internal Training:

    With duration of one month, the first stage consists of the professional’s training to insert them in the Nuclear Medicine sector.

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    Stage 3 – Processes Improvement:

    With duration of 4 months, the third stage is dedicated to improve the processes of the client’s Nuclear Medicine Services.

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    Stage 2 – Learn of the Nuclear Medicine Service:

    With duration of one month, the professional is immersed in the particularities of the client’s Nuclear Medicine Service.

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    Stage 4 – Radiopharmacy Management:

    The fourth and last stage has duration of six months and deals with Radiopharmacy Management.

CONSULTANCY MODULES

RPH SERVICES makes available CONSULTANCY MODULES to adjust the Nuclear Medicine Services to the Radiopharmaceutical Good Manufacturing Practices, according to the requirements in ANVISA’s RDC 38. See below the list of MODULES offered:

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    Consultancy in quality control of radiopharmaceuticals

    Workload of 8 hours;
    Theory and hands-on training in quality control for eluate and radiopharmaceuticals marked with technetium-99.

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    Consultancy in marking and quality control of radiopharmaceuticals

    Workload of 16 hours;
    Theory and hands-on training in quality control for eluate and radiopharmaceuticals marked with technetium-99;
    Assistance in the implementation of the trials in the service’s routine.

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    Consultancy in marking, quality control of radiopharmaceuticals and Good Practices in radiopharmacy (ANVISA’S RDC 38/08)

    Workload of 24 to 32 hours;
    Theory and hands-on training in Good Manufacturing Practices. Approach of elution, marking, quality control, asepsis and processes tracking, since the acquisition until the radiopharmaceutical’s injection. It includes the requirements of the Patient’s National Security Program (Directive 529/2013)

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    Consultancy with management and periodic on-site monitoring of the radiopharmacy and adequacy to RDC 38/08

    Workload: 15 hours per week, for at least 12 months;
    Implementation of Quality gradually and consistently into the radiopharmacy by a RPH qualified professional. It includes all the addressed aspects from the previous modules, as well as team and activities management, radiopharmacy’s stock and costs, trainings, seminars with the team, implementation of new protocols and innovative products.

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    Consultancy with management and periodic on-site monitoring of the radiopharmacy and adequacy to RDC 38/08

    Workload: 15 hours per week, for at least 12 months;
    Implementation of Quality gradually and consistently into the radiopharmacy by a RPH qualified professional. It includes all the addressed aspects from the previous modules, as well as team and activities management, radiopharmacy’s stock and costs, trainings, seminars with the team, implementation of new protocols and innovative products.

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    Tailor-made

    Workload: personalized;
    Identification of the client’s needs and design of a personalized consultancy proposal in radiopharmacy.

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    Consultancy with management and periodic on-site monitoring of the radiopharmacy and adequacy to RDC 38/08

    Workload: 15 hours per week, for at least 12 months;
    Implementation of Quality gradually and consistently into the radiopharmacy by a RPH qualified professional. It includes all the addressed aspects from the previous modules, as well as team and activities management, radiopharmacy’s stock and costs, trainings, seminars with the team, implementation of new protocols and innovative products.

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    Consultancy for implementation of cyclotron

    Workload: Personalized
    Development of a Business Plan, study for implementation, selection of equipment, technical assembly of laboratories.

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