REGULATORY IMPACT ASSESSMENT DALAM PENYUSUNAN SUATU KEBIJAKAN DI BIDANG OBAT KUASI

Authors

  • ERNI RAHMAWATI Badan Pengawas Obat dan Makanan

DOI:

https://doi.org/10.51878/healthy.v2i2.2484

Keywords:

RIA, obat kuasi, BPOM

Abstract

The study aimed to assess the impact of costs and benefits analysis(CBA) as an important step in the Regulatory Impact Assessment (RIA) as part and basic concept of Good Regulatory Practices (GRP) principles. CBA is carried out before a policy concerning stakeholder interests was established. CBA was applied to determined that the policies have been taken had greater benefit compare to impact and cost burden by stakeholders. Therefore the policies can be accepted and can be implemented without obstacles by stakeholders. A CBA survey has been conducted among 61 stakeholders, 80% from business actors. Survey as well as identifying problems faced by business actors during the quasi-drug registration process at the Indonesia FDA (BPOM). In addition, information was collected regarding expectations and suggestions for improvement related to the quasi-drug registration process. Assessment of the impact of costs and benefits (CBA) is carried out on two policy alternatives, namely the first alternative does not require a new policy and the second alternative requires a new policy in the form of quasi-drug regulation. The CBA analysis resulted that the benefits have a better value than the cost, if the policy alternative was taken to develop the quasi drug regulation.

ABSTRAK
Penelitian ini bertujuan untuk menilai manfaat dan dampak biaya (Cost and Benefit Analysis/ CBA) sebagai inti dalam Regulatory Impact Assessment (RIA) sebelum suatu kebijakan ditetapkan. RIA merupakan konsep dasar dalam prinsip-prinsip Good Regulatory Practices (GRP). Penilaian CBA dilakukan sebelum suatu kebijakan yang menyangkut kepentingan luas dari pemangku kepentingan ditetapkan, agar kebijakan memiliki manfaat yang lebih besar dibandingkan dampak biaya yang ditanggung oleh pemangku kepentingan. Sehingga kebijakan dapat diterima dan dilaksanakan tanpa ada hambatan dari pemangku kepentingan. Survei CBA telah dilakukan kepada 61 pemangku kepentingan, 80% adalah pelaku usaha. Survei sekaligus mengidentifikasi masalah yang dihadapi pelaku usaha pada saat proses registrasi obat kuasi di BPOM. Selain itu dikumpulkan informasi terkait harapan dan saran perbaikan terkait proses regsitrasi obat kuasi. Penilaian CBA terhadap manfaat dan biaya (CBA) dilakukan terhadap dua alternatif kebijakan yaitu alternatif pertama tidak perlu ada suatu kebijakan baru dan alternatif kedua, perlunya kebijakan baru berupa peraturan obat kuasi. Hasil analisis CBA diperoleh bahwa manfaat yang lebih baik dibandingkan dampak biaya, apabila alternatif kebijakan yang diambil adalah penyusunan peraturan di bidang obat kuasi.

References

Ando H, Matsui MS and Ichihashi M, (2010). Quasi-Drugs Developed in Japan for the Prevention or Treatment of Hyperpigmentary Disorders. Int J Mol Sci. 2010; 11(6): 2566–2575. Published online 2010 Jun 18. doi: 10.3390/ijms11062566

ASEAN (2017). From https://asean.org/wp-content/uploads/2017/09/ASEAN-Guidelines-on-Good-Regulatory-Practices2.pdf

Azis RA, Olivia F& Arianto H, 2023. Regulatory Impact Assessment (RIA) dalam Perumusan Kebijakan. Lex Jurnalica Vol. 20 Nomor 1, April 2023.

BPOM (2018). Peraturan BPOM Nomor 27 tahun 2018 Tentang Standar Pelayanan Publik Di Lingkungan Badan Pengawas Obat dan Makanan, from https://jdih.pom.go.id/

BPOM (2021). Peraturan BPOM Nomor 10 tahun 2021 tentang Standar Kegiatan Usaha dan Produk pada Penyelenggaraan Perizinan Berusaha Berbasis Risiko Sektor Obat dan Makanan from https://jdih.pom.go.id/

BPOM (2022). Laporan Kinerja Deputi Bidang Pengawasan Obat Tradisional, Suplemen Kesehatan dan Kosmetik (Lakip) Deputi Bidang Pengawasan Obat Tradisional, Suplemen Kesehatan dan Kosmetik.from https://pmpuotskkos.pom.go.id/files/secaraberkala/1.%20LAKIP%20DEPUTI%20II%20TAHUN%202022%20ttd.pdf

Bhandari P and Nikolopoulou K (2020). What Is a Likert Scale? Guide & Examples. Published on July 3. Revised on June 22, 2023. From https://www.scribbr.com/methodology/likert-scale/

ChemLinked. Japan Quasi-drug Regulation from https://cosmetic.chemlinked.com/ cosmepedia/japan-quasi-drug-regulation

Coglianese Cary (2013). Thinking Ahead, Looking Back: Assessing the Value of Regulatory. Korean J. L. & Legis. 5.

Darwinto S (2016). Efektivitas Regulasi dan Pelaksanaan Pengawasan Sumber Daya Perikanan. Studi pada Unit Pelaksana Teknis Stasiun Psdkp Pontianak, Jurnal Mahasiswa S2 Hukum Unversitas Tanjungpura

Databridgemarketresearch (2022). Global Quasi Drugs Market – Industry Trends and Forecast to 2030, Report Nov 2022 From https://www.databridgemarketresearch.com/reports/global-quasi-drugs-market

OECD (2008). Introductory handbook for undertaking Regulatory Impact Assessment (RIA). Organisation for Economic Co-operation and Development. from https://www.oecd. org/gov/regulatory-policy/44789472.pdf

Hasima Rahman (2020). Penerapan Metode Regulatory Impact Assessment Dalam Penyusunan Peraturan Daerah di Kota Kendari . Halu Oleo Law Review. Volume 4 Issue 1, March 2020: pp. 54-71. Halu Oleo Law Review. Faculty of Law, Halu Oleo University, Kendari, Southeast Sulawesi, Indonesia. P-ISSN: 2548-1762 | E-ISSN: 2548-1754. Open Access at: http://ojs.uho.ac.id/index.php/holrev/

LAN (2021). Kick Off Pengukuran Indeks Kualitas Kebijakan Tahun 2021. from https://lan.go.id/?p=7219

LPEM FEB UI Documents. 2019. Program Pelatihan Regulatory Impact Assessment (RIA), Unpublished manuscript, Jakarta.

Peraturan Pemerintah Republik Indonesia Nomor 32 Tahun 2017. Tentang Jenis dan Tarif Atas Jenis Penerimaan Negara Bukan Pajak yang berlaku pada Badan Pengawas Obat dan Makanan, from https://jdih.pom.go.id/

Verico Kiki (2018). Modification of the Regulatory Impact Assessment on Indonesia’s Economic Policies. Economics and Finance in Indonesia Vol. 64 No. 1, June: 43–58 p-ISSN 0126-155X; e-ISSN 2442-9260 43

Wicaksono Dian Agung. (2023). Quo Vadis Pengaturan Regulatory Impact Analysis (RIA) Dalam Pembentukan Peraturan Perundang-Undangan. from https://e-jurnal.peraturan.go.id/index.php/jli/article/viewFile/44/pdf

World Health Organization (WHO) (2017). WHO Global Model Regulatory Framework for Medical Devices including in vitro diagnostic medical devices. from https://apps.who.int/iris/bitstream/handle/10665/255177/9789241512350-eng.pdf

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Published

2023-09-29

How to Cite

RAHMAWATI, E. (2023). REGULATORY IMPACT ASSESSMENT DALAM PENYUSUNAN SUATU KEBIJAKAN DI BIDANG OBAT KUASI. HEALTHY : Jurnal Inovasi Riset Ilmu Kesehatan, 2(2), 99-105. https://doi.org/10.51878/healthy.v2i2.2484

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