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Sukacita dimaklumkan bahawa pada 4 April 2023, Bahagian Regulatori Farmasi Negara (NPRA) telah meluluskan permohonan variasi daripada syarikat Pfizer (Malaysia) Sdn. Bhd., berhubung pengemaskinian tempoh jangka hayat produk Paxlovid seperti berikut:

 

1. Paxlovid (Nirmatrelvir 150 mg Film-Coated Tablets And Ritonavir 100 mg Film-Coated Tablets) (MAL22036001ACRZ)

2. Paxlovid (Nirmatrelvir 150 mg Film-Coated Tablets And Ritonavir 100 mg Film-Coated Tablets) (MAL22036002ACRSZ)

 

 

Kategori

Deskripsi Variasi Yang Diluluskan

MaV-16: Extension of the shelf life of drug product

Memanjangkan tempoh jangka hayat produk (Nirmatrelvir) daripada 18 bulan kepada 24 bulan.

 

Nota:

Sebelum ini, NPRA telah meluluskan pemanjangan jangka hayat daripada 12 bulan kepada 18 bulan pada 11 Oktober 2022.

 

Rujukan:

https://npra.gov.my/index.php/en/component/content/article/427-english/announcement-main/announcement-2022/1527414-pengemaskinian-tempoh-jangka-hayat-antiviral-covid-19-iaitu-paxlovid-daripada-12-bulan-kepada-18-bulan.html?Itemid=1391

 

Bersama ini disenaraikan nombor kelompok dengan tarikh luput baharu yang telah dikemaskini:

 

Bil

Nombor Kelompok

Tarikh Pengilangan

Nirmatrelvir

Tarikh Pengilangan

Ritonavir

Tarikh Luput Pada Label

Tarikh Luput Baharu*

1

FY5877

11-Feb-2022

1-Oct-2021

31-Jan-2023

30-Sep-2023

2

FY8190

11-Feb-2022

1-Oct-2021

31-Jan-2023

30-Sep-2023

3

GA6239

08-Mar-2022

1-Oct-2021

28-Feb-2023

30-Sep-2023

4

GC5599

21-Mar-2022

1-Nov-2021

28-Feb-2023

31-Oct-2023

5

GC8727

29-Mar-2022

1-Nov-2021

28-Feb-2023

31-Oct-2023

6

GC8722

30-Mar-2022

1-Dec-2021

28-Feb-2023

30-Nov-2023

7

GN0918

9-Jun-2022

1-Mar-2022

30-Nov-2023

29-Feb-2024

8

GN0916

23-Jun-2022

1-Mar-2022

30-Nov-2023

29-Feb-2024

 

* Paxlovid adalah produk dengan pek kombinasi melibatkan dua bahan aktif iaitu Nirmatrelvir dan Ritonavir yang mempunyai tarikh pengilangan yang berbeza. Tarikh luput baharu adalah merupakan tarikh luput yang terawal antara dua bahan aktif tersebut.

 

Sekiranya terdapat sebarang pertanyaan lanjut, YBhg. Datuk/ Dato’/ Tuan/ Puan boleh menghubungi One-Stop-Centre di alamat This email address is being protected from spambots. You need JavaScript enabled to view it. atau di talian 03-7883 5400 (sambungan: 4435/4436/4437) atau 03-7801 8445/8446/8447/8449

                                                                                                               

 

Kemaskini: 13 April 2023

 

 

 

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FACT-SHEET-v1.2

 

The infographic above is a summary of activities conducted and coordinated by the Bioequivalence and Ethics Committee (BEEC) Section in 2022. The team consists of six personnel from Bioequivalence and Ethics Committee (BEEC) Section and assisted by eight officers from other sections who are seven officers from the Good Clinical Practice (GCP) & Good Laboratory Practice (GLP) Section and one officer from the Investigational Product Evaluation and Safety section.

In the year 2022, the team managed to conduct 19 inspections which include seven local Bioequivalence (BE) Centre inspections, five foreign BE Centre inspections and seven ethics committee (EC) inspections. Local BE Centre inspections had resumed in February 2022 with all seven inspections done on site either in the Klang Valley or Penang. Of the seven local BE Centre inspected, 5 inspections were surveillance inspections, while the remaining were certification and verification inspections. 

Foreign BE Centre inspections resumed in July 2022 after international travel restrictions were lifted in April 2022. Out of seven planned inspections, the team conducted five on-site inspections all over India including Ahmedabad, Tamil Nadu and Mumbai. Four inspections were certification inspections while one was a surveillance inspection. Two planned inspections were postponed to the year 2023 due to COVID-19. 

There were seven EC inspections done in 2022. Five inspections were surveillance inspections while the two remaining inspections were provisional inspections. Three inspections were carried out on site in the Klang Valley while four inspections were done remotely.

As of November 2022, BEEC had received 621 BEDE (Evaluation of the Need for BE Study Inspection) applications. Of the 621 applications, 65.22% (n=405) had received a decision whereby 58.78% (n=365) were exempted from study-specific inspections and 6.44% (n=40) required study specific inspections. 15.94% (n=99) of applications are currently in the evaluation phase and 2.90% (n=18) applications in the screening phase. Another 15.94% (n=99) of applications were rejected or withdrawn during the screening or evaluation process. All the remaining applications are expected to receive an outcome in the year 2023.

Going into 2023, the team will be looking into optimising the workforce whilst finding the balance between the conduct of inspections and evaluating BEDE applications. BEEC Section will continue to upscale the number of inspections with plans to conduct 29 inspections including local BE Centres, foreign BE Centres and EC inspections in 2023. The majority of these inspections are foreign BE Centre inspections as the team will be focusing on clearing backlog applications from the year 2020 – 2021 brought about by pandemic travel restrictions. The number of BEDE application is also expected to increase in 2023. Process refinements will continue as the team work to ensure that all applications can be reviewed within the specified timeline. The team commits to participation in stakeholder dialogues and involve in trainings for the industry to better support the process optimisation and manage expectations.

 

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Sukacita dimaklumkan bahawa pada 15 Disember 2022, Bahagian Regulatori Farmasi Negara (NPRA) telah meluluskan permohonan variasi daripada syarikat Merck Sharp & Dohme (Malaysia) Sdn. Bhd., berhubung pengemaskinian tempoh jangka hayat produk Lagevrio 200mg Hard Capsule (Bahan Aktif: Molnupiravir 200mg) seperti berikut:

  1. Lagevrio 200mg Hard Capsule (MAL22046001ACRZ)
  2. Lagevrio 200mg Hard Capsule (MAL22046002ACRSZ)
  3. Lagevrio 200mg Hard Capsule (MAL22046003ACRSZ)

Kategori

Deskripsi Variasi Yang Diluluskan

MaV-16: Extension of the shelf life of drug product

Memanjangkan tempoh jangka hayat produk daripada 24 bulan ke 30 bulan

 

Bersama ini disenaraikan nombor kelompok dengan tarikh luput baharu yang telah dikemaskini: 

Bil

Nombor Kelompok

Tarikh Pengilangan

Tarikh Luput Pada Label (24 bulan)

Tarikh Luput Baru (30 bulan)

1

W010954

26 Julai 2021

26 Julai 2023

26 Januari 2024

2

W005186

28 September 2021

28 September 2023

28 Mac 2024

Sekiranya terdapat sebarang pertanyaan lanjut, YBhg. Datuk/ Dato’/ Tuan/ Puan boleh menghubungi One-Stop-Centre di alamat This email address is being protected from spambots. You need JavaScript enabled to view it. atau di talian 03-7883 5400 (sambungan: 4435/4436/4437) atau 03-7801 8445/8446/8447/8449.

 

 

 

National Pharmaceutical Regulatory Agency (NPRA)

Lot 36, Jalan Universiti (Jalan Prof Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.

  • Phone: +603-7883 5400

 

 

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