lavinia – Accestra Consulting https://www.accestra.com Your long term strategic partner for regulatory compliance. Thu, 24 Mar 2022 04:31:40 +0000 en-US hourly 1 https://wordpress.org/?v=6.5.5 https://www.accestra.com/wp-content/uploads/2019/03/cropped-accestra2-32x32.png lavinia – Accestra Consulting https://www.accestra.com 32 32 China Drug Master File (DMF) Filing Webinar for APIs, Excipients & Packaging Materials https://www.accestra.com/china-drug-master-file-dmf-filing-webinar-for-apis-excipients-packaging-materials/ Wed, 31 Mar 2021 03:31:26 +0000 http://www.accestra.com/?p=3635

Join free webinar on China Drug Master File (DMF) Filing for APIs, Excipients & Packaging Materials (click here to register) on Thursday 15th April, 2021, at 10:30 CEST time. The webinar will provide an overview of the requirements, regulatory pathways, how to register your DMF in China and a comparison between US FDA and EMA DMF systems and much more! Accestra and ELC group who are co-hosting, look forward to your participation.

Webinar Topics (30 minutes)

  1. China Regulatory Framework & Registration Pathways
  2. Comparison between China, EU & US
  3. Technical requirements: Pitfalls & Tips
  4. Questions and Answers
  • Date: Thursday 15th April, 2021
  • Time: 10:30 AM CEST
  • Price: Free of charge

Click here to register. You will then receive an invitation to this webinar. Please note that the number of participants is limited.

Presenters

  • Raymond Ng: Business Development Director from Accestra Consulting
  • Chetan Javia: Senior Expert of Strategic Alliance & Regulatory Affairs from ELC Group.

Background

China is one of the fastest growing market for drug APIs, Excipients & Packaging Materials. Due to significant reform, increased demands for pharmaceutical drugs, and increasing government investment in healthcare and R&D, the market is being primed for a major boost in the coming years.

Company introductions

Accestra Consulting Provides China Regulatory Affairs Outsourcing for Drugs/Pharmaceutical, Food and Feed products for China NMPA (Formerly CFDA) regulatory approval including product registration for China, China Drug Master File (DMF) for APIs, Excipient and Packaging Materials and others. For more information you may email: info@accestra.com

ELC Group is a fully-fledged global regulatory partner, working with major pharmaceutical stakeholders for over a decade. ELC provides a range of solutions through 3 divisions: Pharmaceutical, Medical devices and Translations. For more information you may email: info@elc-group.com

]]> Pharmacovigilance (PV) in China https://www.accestra.com/pharmacovigilance-pv-in-china/ Sat, 13 Mar 2021 05:53:55 +0000 http://www.accestra.com/?p=3564
 
Before 2018, the Pharmacovigilance (PV) System in China was still in its early days. Companies’ activities to drug safety were for the most part passive.
 
Then market authorization holder (MAH) was put in place to report on adverse drug reactions (ADR).
 
As a result, in 2019 China included the provision of “establishing Pharmacovigilance System” in its Supreme Law of Pharmaceutical Supervision & Management: “China Drug Administration Law.”
 
Shortly afterward it released “Good Pharmacovigilance Practice” (GVP, draft version for public comments) to standardize the responsibilities of MAH in PV at the end of 2020. This marked a new chapter of PV in China.
 
The GVP states that companies need to conduct a comprehensive drug safety evaluation and PV audit during the life cycle of a drug product. This is to reduce drug safety risks and promote public health.

What is Pharmacovigilance (PV)

Pharmacovigilance (PV) is:
  • the monitoring,
  • identification,
  • evaluation,
  • and control of adverse drug reactions (ADRs).
This also includes other harmful reactions related to drug use.
 
PV expands the scope in how ADRs are monitored and plays a part in the life cycle of a drug product from clinical trials through post-marketing.
The period to conduct pharmacovigilance audit in the life cycle of a drug prodcut.
Fig. 1: The period to conduct pharmacovigilance audit in the life cycle of a drug product.

History of Pharmacovigilance (PV) in China

China was late in its Pharmacovigilance work, which happened in three stages:
 

Stage One

1988 – 2011
China joined WHO-PIDM in 1998 and began to establish ADR system. Authorities encouraged companies to report ADRs, without regular inspection.
 

Stage Two

2011 – 2018
Regulations stipulated that companies need to establish their ADR System. Guidelines for inspection of reporting and monitoring of ADRs were released in 2015 to strengthen supervision to companies’ activities on ADR.
 

Stage Three

2018 – present
NMPA specified in 2018 that MAH should be responsible in reporting ADRs.
 
In 2019, Pharmacovigilance (PV) was written in the newly established Drug Administration Law for the first time.
 
Regulations and laws emphasized the significance of risk management of drugs pushing companies to prioritize PV.
 
The history of Pharmacovigilance (PV) in China

Important Regulatory Milestones

Ministry of Health

2011 – Measures for the reporting and monitoring of Adverse Drug Reaction.
ADR reporting system is established.

CFDA

2015 –  Guidelines on inspection of the reporting and monitoring of adverse drug reactions (for trial implementation)
The monitoring, supervision, and inspection of ADR are strengthened.

State Council

2017 – Agenda of deepening reform of the examination and approval system and encouraging innovation of drugs and medical devices.
The system of MAH directly reporting ADRs is established.

NMPA

2018 – Announcement on Direct Reporting of Adverse Drug Reaction by Marketing Authorization Holder.
The responsibility of MAH in reporting ADRs is implemented.

Congress

2019 – Drug Administration Law.
PV is written into the basic law for the first time.
The main responsibilities of MAH in PV are emphasized.

NMPA

2020 – Good Pharmacovigilance Practices (draft for comments)
The main responsibilities of MAH in PV are standardized. Post-marketing management is strengthened.

Laws and regulations of pharmacovigilance in China.

Post-marketing Responsibilities of MAH in PV

1. Establishment of PV System

  • Choose persons in charge of ADR monitoring.
  • Establish specialized departments.
  • Appoint specialists.
  • Set up and improve relevant management systems.
 
Monitor, identify, evaluate and control ADRs and other harmful reactions related to drug use through comprehensive and effective management and maintenance system.
 

2. Monitor and Report ADRs

  • Establish channels for collecting ADR information.
  • Actively collect suspected adverse reactions from drug use in a comprehensive manner.
  • Report ADRs in time as required.
 
Channels to collect ADRs include:
  • Medical facilities,
  • enterprises,
  • phones,
  • academic literature,
  • post-marketing safety studies and projects,
  • overseas information.
 

3. Identify and assess safety risks

  • Identify potential risks of drugs and conduct studies on the mechanism and causes of those risks.
  • Actively carry out post-marketing safety studies.
  • Conduct ongoing risk evaluation and benefits of drugs.
  • Prepare and submit annual reports and Periodic Safety Update Reports (PSUR).
 

4. Risk Control of Drug Safety

If the listed drugs have significant risks according to the results of risk assessment, a PV plan must be made, modified and implemented, and updated in a timely manner according to the changes of risk perceptions.
 

5. Create and maintain PV System Master Files (PSMF)

  • Create and maintain PV system master files to describe the PV system and activities.
  • Update the master files on time to ensure that they are consistent with the current PV system and activities, and conform to relevant laws and regulations, and practical work requirements

Services Accestra Consulting Group can provide

We provide services for Post-marketing Pharmacovigilance (PV) related activities in China, including:

  • Establishment and Improvement of Post-marketing PV System.
  • Processing of Post-marketing Individual Case Safety Reports (ICSRs).
  • Medical Literature Searching.
  • Periodic Safety Update Report (PSUR) Preparation.
  • Safety Annual Report Preparation.
  • PV System Master Files (PSMF) Preparation & Update on behalf of the client.
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