Certification in Distribution and Wholesaling Pharmaceutical Best Practice

Program ID: CDWP

Package Geographical Regions: All regions

GBP 1250.00

GBP 1250.00

Distribution and Wholesaling Pharmaceutical Best Practice Package

The International Academy of Pharmaceutical Practice will provide Continued Professional Development/ Continuing education courses enabling Practicing Pharmacist to apply World Health Organisation Best Pharmaceutical Practice standards to ensure that safe, effective, and quality medicines are provided to patients worldwide.

These courses will review the WHO international Guidelines issued to assist Member States to obtain medicines having the required standards of Quality, Safety and Efficacy and we shall highlight the essential practices requirements for the Procurement , distribution and supply chain management of Medicines to assure that All Patients worldwide have access to medicines that meet international standards and that adulterated and counterfeit medicines are excluded ,which account for an unacceptable level of suffering to the patient.

All IAPP eLearning courses aim to contribute to the World Health Organization (WHO) objectives for greater Patient Safety and the courses available in the Distribution and Wholesaling Pharmaceutical Best Practice Package will help to;

  • Eradicate the  10-15% and up to 50% of medicines in the medicines supply chain that are adulterated or counterfeited.
  •  The Global cost associated with medication errors has been estimated by the WHO to cost $ 42bn/year.
  • Reduce the costs of medicines by streamlining the supply chain between Manufacturer and Patient, illuminating secondary wholesalers who fail to add value to the product

This Program Includes:
  1. New Developments in The Practice of Pharmacy CPD / CE

    This course identifies the changes in Pharmacy Practice standards and introduces the measures necessary to improve Pharmaceutical Practice standards to achieve the Quality ,safety and efficacy necessary for a Patient focused Service in the future

    This e-lecture identifies the principal drivers for change in the Practice of Pharmacy and proposes ways in which the Pharmacy workforce may adapt to changes in the practice standards to ensure that all Patients receive “Medication Without Harm” in line with the WHO directive 2020. This course identifies the additional skills required by the Pharmacy workforce for working in each of the sectors of pharmacy, and specifies the additional learning as part of the Continued Professional Development.

    Credits: 3 CPD / CME

    No. of Hours: 3 hrs

    Learning Objectives: 

    This training course introduces the skills required to be able to take advantage of the “New Developments in Pharmacy Practice" and to introduce the Four Principal changes required to be made to the Practice of Pharmacy in order to assure greater care and safety of Patients.
    The four Principal changes required in the Practice of Pharmacy are as follows.

    • Support the technology which has lead Development of Biopharmaceutical products that has led to development of the Covid-19 vaccine and Personalised medicine such as treatment for cystic fibrosis.  
    • Adopt the use of Artificial Intelligence, and Manufacturing Intelligence to provide information to allow for improved diagnosis and treatment.
    • To improve Quality and Safety of medicines in the Global supply chain by excluding adulterated and counterfeit medicines and providing traceability of the origin of medicines to identify the sources of those drugs that provide unexpected adverse events 
    • Improve the Affordability of essential drugs by rationalizing the manufacture and distribution of medicines and eliminating all non-value adding activity ensuring that lifesaving medicines are available to all.

    The IAPPS training program if followed will help to ensure the achievement of the above 4 objectives over the next decade

    Who Should Enroll:

    Registered pharmacist practitioners, pharmaceutical scientists, pharmacy technicians and other pharmacy support workforce cadres, pre-service students/trainees) working in a diversity of settings (e.g. community, hospital, research and development, industry, military, regulatory, academia and other sectors) with a diversity of scope of practice 

    Click To Buy
  2. Current Issues with the Medicine Supply Chain CPD / CE

    This course identifies the changes in Pharmacy Practice standards and introduces the measures necessary to improve Pharmaceutical Practice standards to achieve the Quality ,safety and efficacy necessary for a Patient focused Service in the future

    This course will review the potential treats to the Global Medicines Supply Chain and identify the measures necessary to exclude Counterfeit and adulterated medicines and improve delivery performance bay using Block chain technology and Vendor qualification to verify quality  and Enterprise Resource Planning to improve delivery performance of medicines and a clear understanding of the principals of supply chain management.

    Credits: 6 CPD / CME

    No. of Hours: 6 hrs

    Learning Objectives: 

    On completion of this course the delegate will have an understanding of

    • Stock shortages and the measures necessary to avoid
    • Measures necessary to exclude of counterfeit and adulterated medicines
    • The application of Block Technology and Track and trace to verify the origin of stock
    • The application of ERP software to carry out the processes of; Product requestioning Planning process - Procurement and Purchasing -Vendor qualification & Quality Management and controlled distribution to wholesalers.
    • The application of LIMS (Logistics Information Management Software) to manage stock in Hospital and Community Pharmacies

    Who Should Enroll:

    ALL Persons involved in the Practice of Pharmacy which should include – Pharmaceutical Production, Distribution, Wholesale, Hospital and Community Pharmacies who are Dispensing medicines to the patient

    Click To Buy
  3. The Convergence of Digital Technologies and Pharmaceutical Practice CPD / CE

    This eLearning training course will address the benefits of applying Digital technology to the electronically recorded health care records to improve diagnosis and treatment ,ensuring the effectiveness of medicinal treatment that is made available to all Patients who may require.

    This eLearning training course will address the benefits of applying Digital technology to the electronically recorded health care records to improve diagnosis and treatment ,ensuring the effectiveness of medicinal treatment that is made available to all Patients who may require.

    Credits: 4 CPD / CME

    No. of Hours: 4 hrs

    Learning Objectives: 

    On completion of this course the delegate will have an understanding of how the application of  Artificial Intelligence- Machine Learning and Deep Learning to the Electronic health records ,that will provide Digital Healthcare solutions to enable the development of Personalized medicine, secure quality of medicines in the supply chain and facilitate the safe and effective treatment of patients.

    Who Should Enroll:

    ALL Persons involved in the Practice of Pharmacy which should include – Pharmaceutical Production, Distribution, Wholesale, Hospital and Community Pharmacies who are Dispensing medicines to the patient

    Click To Buy
  4. What you need to know about Pharmaceutical Quality Management Systems CPD / CE

    Significant increases of adulterated and counterfeit Drugs entering the medicines supply chain due mainly to a failure in the Quality management stem, which requires to be corrected by all persons responsible for the distribution of medicines. This course will provide the Essential Practice standards to ensure that medicines have been produced in accordance with the international Quality Management Standards to ensure patient safety.

    Significant increases of adulterated and counterfeit Drugs entering the medicines supply chain due mainly to a failure in the Quality management stem, which requires to be corrected by all persons responsible for the distribution of medicines.

    A Quality Management System (QMS) is a collection of processes focused on consistently achieving the quality objectives and are expressed as the organizational structure, policies, procedures, processes and resources needed to provide patients with a Quality Service.

    This course combines the technical requirements of Good Pharmaceutical Practice as stated in ICH Q10 with the business needs of ISO 9001 and applies them to the management of pharmaceutical products supplied to patients

    Credits: 4 CPD / CME

    No. of Hours: 4 hrs

    Learning Objectives: 

    This course has been prepared in accord with the latest WHO Good Pharmaceutical Practice standards for ensuring that all dispensed Medicines meet the required standards of Quality, Safety and Efficacy as defined by the WHO Annex 1 Quality Management covering a number of factors, which ensures the quality of medicines and Patient safety.

    Who Should Enroll:

    ALL Persons involved in the Practice of Pharmacy which should include – Product Development, Clinical assessment, Manufacturing, Distribution, Hospital and Dispensing medicines to the patient

    Click To Buy
  5. Principals and Techniques of the Quality Risk Management CPD / CE

    Principals and Techniques of the Quality Risk Management are required to determine if a Product or Process deviation presents a potential risk to the Patient and if so, how it can be mitigated to ensure the patients safety.

    Principals and Techniques of the Quality Risk Management are required to determine if a Product or Process deviation presents a potential risk to the Patient and if so, how it  can be mitigated to ensure the  patients safety.

    This eLearning course provides the principles and tools which can be used to Manage the Risk to Quality of Medicines which can be applied to different aspects of pharmaceutical quality.

    This includes all aspects involved in the Development , manufacture and supply of drug substances to assure the Quality Safety and Efficacy of medicines for Patients

    Credits: 4 CPD / CME

    No. of Hours: 4 hrs

    Learning Objectives: 

    This course will provide an introduction to the skills and competencies required, to Assess and control out of specification and Product/Process deviation by Quality Risk Management. The candidate will learn how to asses and mitigate risk by using techniques such as Risk cause analysis and failure mode Effect analysis to identify and mitigate the potential risk.

    Who Should Enroll:

    Persons  involved in Pharmaceutical Processes – Product Development, Clinical assessment, Manufacturing , Distribution, Pharmacovigilance, and Dispensing medicines to the patient

    Click To Buy

John Dr Jolley FR PHARM S, FCQI CQP

Is a Pharmaceutical Consultant providing technical consultancy and bespoke training solutions to the Pharmaceutical Profession, he has a degree in Pharmacy and has been awarded fellowships with the Royal Pharmaceutical Society and Chartered Quality Institute as a consultant lead assessor.

I obtained a BSc Pharm Hons degree in Pharmacy, and a research fellowship at Boots research Nottingham working on formulation development, during which time I published several technical papers.

I joined Beecham Products UK as a management Trainee and was later appointed General Manager of a Beecham subsidiary in Ireland, returning to Beecham Head Quarters in London, where I worked as special products adviser to the Divisional Managing Director for Beecham Products.

I was invited to join Boehringer Ingelheim (UK) Ltd as Technical Director and remained there for 15 years before leaving to establish “Pharma Consult” an International technical and training consultancy working with associates in the US- Latin America- Asia Specific, Saudi Arabia and Other GCC countries, and India.
I have held positions with responsibility for; Clinical Research, Product Registration, Manufacturing, Distribution, Quality Assurance, and General Management, and am a practicing Qualified Person (QP) with experience if working in Biotech industry.

I was awarded Fellowship with the Royal Pharmaceutical Society (UK) and in 2003 was elected to serve on the council of the RPS(UK) as their treasurer. In 1998 I became Consultant Lead assessor of the Chartered Quality Institute and in 2015 was invited to join the worshipful Society of Apothecaries and granted the freedom of the City of London


 
Steve Jolley 

Steve Jolley is a subject matter expert in all areas of global safety compliance and signal detection, and is a frequent speaker at leading industry events.

Steve has 35 years’ experience in drug safety & pharmacovigilance and has worked with over 250 clients in North America, Europe, Japan, India, China, the Middle East and Africa. He holds degrees in mathematics and computer science from Cambridge University, England. He is an Adjunct Professor at Rutgers University and teaches part of their Master's degree in Drug Safety and Pharmacovigilance.

Steve is a featured speaker with FDA, EMA and MHRA at conferences and webinars on auditing, signaling and data mining. He is a member of DIA’s training faculty and is an instructor for DIA’s Clinical Safety and Pharmacovigilance Certificate Program. In 2010 Steve was elected as chairman of the DIA’s Clinical Safety and Pharmacovigilance steering committee for North America.

Steve began his career in the pharmaceutical industry in 1985 when he founded DLB Systems, a supplier of computer systems for clinical trials and adverse event reporting to many of the leading life science companies worldwide. DLB was acquired by eResearch Technologies in 1997; since then Steve has worked as an independent consultant.


 

Program Highlights
Duration: 22 hrs
Released On: 09/01/2021
Downloadable Resources: 
Case Studies: 
Need Help?

We can walk you through your program options and Subscriptions please contact us