This was presented at mySociety's TICTeC Show & Tell event, which was held virtually on 23rd March 2021. More details on the event can be found here: https://tictec.mysociety.org/showandtells/2021
Medical Delivery App or Pharmacy App Development - Idea Usher Nitish Garg
To Read More Visit our Blog: https://ideausher.com/iot/medicine-delivery-app/
Our Website - www.IdeaUsher.com
1. How does application work for customers?
2. How does application work for administrators?
3. Cost of medicine App development
4. The team required to build such an App (App developer, quality analyst, UI/Ux Designer).
online pharmacy app development solution, Online pharmacy. online medical store, pharmacy app, Best pharmacy app.
Online doctor consultation app doctor appointment booking appAPPNWEB Technologies
We are here to development Doctor Appointment Booking Mobile App for you. if you want to develop it for your business, know about to it's Benefits, Market overview and cost of development.
For More Info:- https://www.appnwebtechnologies.com/blog/doctor-appointment-booking-app-development-a-run-through/
Medical Delivery App or Pharmacy App Development - Idea Usher Nitish Garg
To Read More Visit our Blog: https://ideausher.com/iot/medicine-delivery-app/
Our Website - www.IdeaUsher.com
1. How does application work for customers?
2. How does application work for administrators?
3. Cost of medicine App development
4. The team required to build such an App (App developer, quality analyst, UI/Ux Designer).
online pharmacy app development solution, Online pharmacy. online medical store, pharmacy app, Best pharmacy app.
Online doctor consultation app doctor appointment booking appAPPNWEB Technologies
We are here to development Doctor Appointment Booking Mobile App for you. if you want to develop it for your business, know about to it's Benefits, Market overview and cost of development.
For More Info:- https://www.appnwebtechnologies.com/blog/doctor-appointment-booking-app-development-a-run-through/
The Clinical Laboratory Improvement Amendments (CLIA) regulate laboratory testing and require clinical laboratories to be certificated by their state as well as the Center for Medicare and Medicaid Services (CMS) before they can accept human samples for diagnostic testing.
This PDF will discuss the key information that is required for a medical device 510k submission. The information presented in this PDF pertains to just one of the many best practices in a medical device 510K preparation and submission.
In this presentation we want to outline the principles of medical device regulations and the 510(k) Premarket notification process for an efficient product approval with the FDA.
Webinar or Online Training on A comprehensive overview of 510(k) submissionComplianz World
Complianz World is a US based company, and a leading GRC training provider has announced to conduct
Webinar or Online Training on
A comprehensive overview of 510(k) submission
CMS BlueButton On FHIR for Researchers - Presentation to NIH and PCORI Resear...Mark Scrimshire
This is a presentation given to researchers from PCORI and NIH (Precision Medicine Initiative) about the potential benefits to researchers that comes from letting CMS Medicare Beneficiaries share their Claims information with a research study using the Proposed CMS BlueButton data formats built on the HL7 Fast Health Interoperability Resources Specification.
A complete guide on how to develop an on demand medicine delivery solution fo...Yelowsoft
We are living in a digital age where we can have almost anything by just making a few taps on our phone. On-demand delivery services have certainly increased our appetite for instant gratification even for the things which are not needed on an instant basis. But what about the things which are sometimes needed on an instant basis? Shouldn’t they be available at our fingertips?
Building a pharma delivery app: To ensure smooth delivery of medicinesVishal Sinhasan
Tap a few times on your phone screens and you can order food. Tap some more and you can get a cab at your doorstep. You can even get on-demand home cleaning services or order pharma delivery from your phone and it is the new way of life for us all.
Commercial medical devices in Colombia require registration with INVIMA (Instituto Nacional de Vigilancia de Medicamentos y Alimentos), the country’s medical device regulator. Classification of devices in Colombia follows a four-tiered risk model (Class I, Class IIa, Class IIb and Class III). Colombia’s device classification system is similar to those of the European Union and other Global Harmonization Task Force (GHTF) systems. If the device falls into a lower-risk category in Colombia (Class I or IIa), the company will qualify for an automatic certificate upon notification to INVIMA —it will be able to sell its devices immediately.
Regulatory Concerns When Running Virtual/Paperless Clinical TrialsTarget Health, Inc.
With drug and device manufacturers and the U.S. Food and Drug Administration (FDA) supplying much of the push, so-called paperless clinical trials are gaining momentum. In this eClinical Forum webinar, Dr. Jules Mitchel, President of Target Health, facilitated the discussion on the future landscape and regulatory concerns of paperless clinical trials and clinical trial design incorporating mobile tools.
How Medicine Delivery Apps Can Transform Healthcare EMed Pharmatech
Medicine delivery apps are electronic replacements for brick-and-mortar pharmacies. In this blog, we chart the phenomenal rise of medicine delivery app development, and how medicine delivery applications are fast becoming a go-to solution in the digital healthcare landscape.
If you are looking to find integrated medicine delivery app development solutions for your healthcare business, feel free to contact us at EMedStore.
#uae #egypt #iraq #iran #jordan #kuwait #lebanon #libya #oman #qatar #saudiarabia #yemen #islamicrepublic #emedstore #digitalhealth #digitalhealthcare #doctorapp #patient #doctor #health #healthcareIT #telemedicine #epharmacy #medicinedelivery #onlinepharmacy #Integration #labapplication #b2bpharmacy #healthcare
View Source:
https://www.emedstore.in/blog/Post/medicine-delivery-apps-transform-healthcare/228
The Clinical Laboratory Improvement Amendments (CLIA) regulate laboratory testing and require clinical laboratories to be certificated by their state as well as the Center for Medicare and Medicaid Services (CMS) before they can accept human samples for diagnostic testing.
This PDF will discuss the key information that is required for a medical device 510k submission. The information presented in this PDF pertains to just one of the many best practices in a medical device 510K preparation and submission.
In this presentation we want to outline the principles of medical device regulations and the 510(k) Premarket notification process for an efficient product approval with the FDA.
Webinar or Online Training on A comprehensive overview of 510(k) submissionComplianz World
Complianz World is a US based company, and a leading GRC training provider has announced to conduct
Webinar or Online Training on
A comprehensive overview of 510(k) submission
CMS BlueButton On FHIR for Researchers - Presentation to NIH and PCORI Resear...Mark Scrimshire
This is a presentation given to researchers from PCORI and NIH (Precision Medicine Initiative) about the potential benefits to researchers that comes from letting CMS Medicare Beneficiaries share their Claims information with a research study using the Proposed CMS BlueButton data formats built on the HL7 Fast Health Interoperability Resources Specification.
A complete guide on how to develop an on demand medicine delivery solution fo...Yelowsoft
We are living in a digital age where we can have almost anything by just making a few taps on our phone. On-demand delivery services have certainly increased our appetite for instant gratification even for the things which are not needed on an instant basis. But what about the things which are sometimes needed on an instant basis? Shouldn’t they be available at our fingertips?
Building a pharma delivery app: To ensure smooth delivery of medicinesVishal Sinhasan
Tap a few times on your phone screens and you can order food. Tap some more and you can get a cab at your doorstep. You can even get on-demand home cleaning services or order pharma delivery from your phone and it is the new way of life for us all.
Commercial medical devices in Colombia require registration with INVIMA (Instituto Nacional de Vigilancia de Medicamentos y Alimentos), the country’s medical device regulator. Classification of devices in Colombia follows a four-tiered risk model (Class I, Class IIa, Class IIb and Class III). Colombia’s device classification system is similar to those of the European Union and other Global Harmonization Task Force (GHTF) systems. If the device falls into a lower-risk category in Colombia (Class I or IIa), the company will qualify for an automatic certificate upon notification to INVIMA —it will be able to sell its devices immediately.
Regulatory Concerns When Running Virtual/Paperless Clinical TrialsTarget Health, Inc.
With drug and device manufacturers and the U.S. Food and Drug Administration (FDA) supplying much of the push, so-called paperless clinical trials are gaining momentum. In this eClinical Forum webinar, Dr. Jules Mitchel, President of Target Health, facilitated the discussion on the future landscape and regulatory concerns of paperless clinical trials and clinical trial design incorporating mobile tools.
How Medicine Delivery Apps Can Transform Healthcare EMed Pharmatech
Medicine delivery apps are electronic replacements for brick-and-mortar pharmacies. In this blog, we chart the phenomenal rise of medicine delivery app development, and how medicine delivery applications are fast becoming a go-to solution in the digital healthcare landscape.
If you are looking to find integrated medicine delivery app development solutions for your healthcare business, feel free to contact us at EMedStore.
#uae #egypt #iraq #iran #jordan #kuwait #lebanon #libya #oman #qatar #saudiarabia #yemen #islamicrepublic #emedstore #digitalhealth #digitalhealthcare #doctorapp #patient #doctor #health #healthcareIT #telemedicine #epharmacy #medicinedelivery #onlinepharmacy #Integration #labapplication #b2bpharmacy #healthcare
View Source:
https://www.emedstore.in/blog/Post/medicine-delivery-apps-transform-healthcare/228
Bring your pharmacy business to a new level by offering medicine delivery. For this purpose, you need to develop a medicine delivery app. And here's how to do that.
Horn of africa conference and expo, presentation on the regulatory framework for medical devices in kenya with the new guidelines requirement starting January 2019
HIPAA HITECH Privacy & Security Rules for E-prescribing
Disclaimer
The materials available on this document and web site are for informational purposes only and not for the purpose of providing legal and or clinical advice.
You should contact your attorney and information security officer to obtain proper advice with respect to any particular issue or problem. Use of and access to this document or any of the e-mail links, materials, etc., contained within the document do not create an attorney-client relationship, consulting between the authors, legal and / or medical advice . between the user or browser. Only guidance from U.S. Government agencies directly should be used.for decision making.
On demand medicine delivery app is an innovative solution that allows you to buy medication right at your door step. The On Demand Medicine app has been used by consumers that want to be more involved in their healthcare decisions and are seeking more personalized feedback on products, services and diagnoses. Today technology is growing very fast.
Future Innovation In Health Sector With On-Demand Medicine Delivery Apps For ...Cerebrum Infotech
Cerebrum infotech provide the best on demand medicine delivery apps for business solution, as they provide a secure platform for consumer connection. To know more, read our blog today!
The medical device industry is constantly looking for innovative new ways to treat and cure conditions. Last month, the FDA permitted marketing of the first-ever game-based digital therapeutic device aimed at treating children with attention deficit hyperactivity disorder (ADHD). The prescription-only video game, in combination with other treatments, is engineered to create physiological changes in the brain to improve cognitive function...
Good regulatory practice are internationally recognized process, system, tools and method for improving the quality of regulation.
It includes
1)COMMUNITY PHARMACY RETAIL AND WHOLESALE PHARMACY
-Dacumentation
-Licenses
-Renewal
-E-governance
2) HOSPITAL PHARMACY
-Dacumentation
-Licenses
-Renewal
-E-governance
3) PHARMA MANIFACTURING
-Dacumentation
-Licenses
-Renewal
-E-governance
4) IMPORT OF DRUG AND MEDICAL DEVICE
-Dacumentation
-Licenses
-Renewal
-E-governance
5) EXPORT OF DRUG AND MEDICAL DEVICE
-Dacumentation
-Licenses
-Renewal
-E-governance
Mera Medicare (One of the fastest growing Healthcare start-up) is currently operational in Delhi-NCR and Bangalore and going live in 15 more cities in 2015 (Mumbai, Pune, Hyderabad, Jaipur, Chennai, Coimbatore, Mysore, Raipur, Indore, Ranchi, Bhopal, Nashik, Nagpur etc.)
How Decision-Support Tools Cure the Prior Authorization Time DrainCognizant
A collaboration between Cognizant, the New England Healthcare Exchange Network and Informatics In Context is demonstrating how a real-time prior authorization (PA) system for medical and administrative processes saves time and money.
Indian regulatory requirements - industrial pharmacy 2Jafarali Masi
Indian Regulatory Requirements: Central Drug Standard Control Organization (CDSCO) and State Licensing Authority: Organization, Responsibilities, Certificate of Pharmaceutical Product (COPP), Regulatory requirements and approval procedures for New Drugs
Similar to Civic tech vs. illicit pharmacies - Ibraheem Saleem (Code for Pakistan) (20)
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2. The Problem
Illegal pharmacies are a big problem in Pakistan:
● In the KP province there are only 50 drug inspectors who are required to check more than 12,000
registered chemist shops
● In 66,879 inspections carried out from 2014-2018, 1,471 drugs were declared substandard and 146
spurious, 2,322 pharmacies were sealed, 72 FIRs were registered and 544 cases were decided by
courts with the convicts being awarded fines and jail sentences (source: Dawn News)
● More than 600 drug licences issued in Peshawar were found to be fake on verification (source: Dawn
News)
3. Issues and Challenges
There were numerous issues and challenges in the pharmaceutical sector of the KP province. On one hand the health
department faced issues in tracking duplicate and fake licenses and on the other hand there were no centralized online
systems where drug store owners could apply for licenses online.
There was a need for an online platform where:
Users could easily
apply for licenses
Department could
check duplicate and fake licenses
Tracking the progress of
each license would be easy
4. KHYBER PAKHTUNKHWA
GOVERNMENT INNOVATION
FELLOWSHIP PROGRAM
Selecting the Problem Statement
The Fellowship team received a request from the Department of
Health KP to digitise and automate the pharmaceutical license
registration, renewal and verification process.
The Fellowship team selected the problem statement under the 6th
cycle of the Fellowship program which was executed from
June-November of 2020.
A team of three Fellows were assigned to the department to
develop a digital system for pharmaceutical license registration and
make the entire process digital.
5. The KP Government Innovation Fellowship Program is a 6-month program supported by Code
for Pakistan, the KP IT Board, and The World Bank
Empowering
Government
Increasing Citizen
Reach
Creating Efficiency in
Govt. Processes
Increasing Govt.
Transparency
The Fellowship Program - Key Focus Areas
6. The Fellows
Muhammad Awais Khan
(Full Stack Developer)
Asfandiyar
(Full Stack Developer)
Abbas Khan
(UX/UI Designer)
7. Conducting User Research
The Fellows conducted a user-research survey from a sample size of 50 respondents
(pharmacy-owners). The figures illustrate the key findings of the user research survey
Average time taken for license issuance Perception of manual processing
8. Developing a Solution
The Fellows developed a fully centralized online platform that can digitise the entire process for license
application, renewal and verification for pharmacies across the KP province. The online system has four main
modules:
Pharmacy Council
Module
1
Applicant
Module
2
DG Drugs
Module
3
Inspector
Module
4
Administrator Module
9. Applicant/Proprietor applying for
pharmacy license
AFTER SCRUTINY THE PHARMACY
LICENSE IS AWARDED
USER APPLIES FOR LICENSE ONLINE
APPLICATION IS RECEIVED BY DG
DRUGS DEPARTMENT
APPLICATION IS ASSIGNED TO DRUG
INSPECTOR
● DG Drugs
Department receives
the application
● The submitted
documentation is
checked against
pharmacy council
records
● If documents are valid
the application is
forwarded to Drug
Inspector
● User creates
account on the
online portal
● User submits
documents and
selects license
category
● User submits
application
● Drug Inspector
receives the
application
● Drug Inspector is
required to make a
field visit to check the
drug store location
and its condition
● Drug Inspector can
reject application if
the pharmacy is
substandard
Applicant is awarded
pharmacy license if the
application fulfills the
acceptance criteria
User Journey Map
users can track application status
10. System’s Security Features
Unique Tracking IDs Numeric Captcha
Codes
Data Encryption Using QR Codes
Online System’s Security Features:
These security features ensure that the data remains safe and only valid licenses
are issued
11. Pharmacy Inspection App
Drug Inspectors conduct field visits to the pharmacy for
checking documents, pharmacy location and facilities. These
checks are made through the field inspection mobile app
Verifying documents Checking medicines
and facilities
Taking geo-coordinates
of pharmacy location
12. Generating Tamper-Proof Pharmacy License
Digitally generated QR code
Allotted license number
generated through Unique ID
and Random Number
Digital signature
Qualified person digital photo
System generated validity date
13. Open Source Solution
View project on GitHub
The online system is accessible on an internet connected laptop, tablet and mobile phone. Moreover the online system
has been developed using open source libraries and tools and the project has been licensed under the MIT License (MIT).
14. Impact so Far
Over 15,000 manual records
of qualified persons digitized
Consumers can check
authenticity of licenses by
scanning QR-codes
20 Govt. officials trained
Time reduced to acquire a
license from 1 month to 10
days
Department received a low
cost sustainable solution
15. KP Government Innovation Fellowship Program
codeforpakistan.org/programs/fellowship/
/codeforpakistan
/codeforpk