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Recommendations to the Sponsors for managing of Clinical Trials during the COVID-19 pandemic and the declared State of emergency in the Republic of Bulgaria
EMA gives advice on the use of non-steroidal anti-inflammatories for COVID-19
Reporting suspected side effects of medicines in patients with COVID-19
New measures to avoid handling errors with leuprorelin depot medicines
CTIS Highlights
PRAC recommends revoking marketing authorisation of ulipristal acetate for uterine fibroids
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Issue of Authorization for extension of the range of the issued Marketing Authorization of pharmaceutical product
Issue of Variation to a Registration Certificate for wholesale of pharmaceutical products on the territory of the Republic of Bulgaria
Issue of Marketing Authorization for production of pharmaceutical products, active substances used as starting materials and medicinal products for clinical trial
Issue of Variation of Marketing Authorization of pharmaceutical product for transfer of the rights over an issued Marketing Authorization of medicinal product
Issue of Marketing Authorization for conduction of clinical trial of medicinal product
Issue of Marketing Authorization for production of pharmaceutical products, for active substances used as starting materials and for medicinal products for clinical trial
Issue of Variation to a Marketing Authorization for wholesale of pharmaceutical products
Issue of Marketing Authorization for wholesale of pharmaceutical products
Issue of Marketing Authorization of pharmaceutical product via Decentralized Procedure
Issue of Marketing Authorization of pharmaceutical product via Mutual Recognition Procedure
Issue of Marketing Authorization of pharmaceutical product via National Procedure
Issue of Certificate for pharmaceutical product
Issue of Exemption Certificate of batch of pharmaceutical product under article 70 of the Law on Medicinal Products in Human Medicine (LMPHM)
Issue of Certificate for the origin of the pharmaceutical product
Issue of Certificate for registration of pharmacy
Issue of registration certificate for homeopathic pharmaceutical product
Issue of Registration Certificate for wholesale of pharmaceutical products on the territory of the Republic of Bulgaria
Issue of Variation to a Registration Certificate for wholesale of pharmaceutical products on the territory of the Republic of Bulgaria
Registration of medical devices
Issue of report for information received in BDA for adverse drug reactions (ADR) for a pharmaceutical product
Issue of Variation to a Marketing Authorization Type II to the Marketing Authorization of pharmaceutical product
Issue of approval of pharmaceutical clinical trial
Issue of Marketing Authorization for pharmaceutical clinical trial under art. 109 item 2 of the Law on Medicinal Products in Human Medicine (LMPHM)
Issue of Marketing Authorization for significant change in a pharmaceutical clinical trial under art. 109 item 2 of the Law on Medicinal Products in Human Medicine (LMPHM)
Approval of non-interventional pharmaceutical clinical trial
Issue of Marketing Authorization for import of pharmaceutical products, active substances used as starting materials and medicinal products for clinical trial
Issue of Registration Certificate for wholesale of medicinal products on the territory of the Republic of Bulgaria
Issue of Variation to a Certificate for registration of pharmacy
Issue of Exemption Certificate of batch of pharmaceutical product under article 69 of the Law on Medicinal Products in Human Medicine (LMPHM)
Issue of Marketing Authorization for wholesale of medical devices
Issue of Variation to a Marketing Authorization for wholesale of medicinal products
Issue of addendum to the Marketing Authorization for conduction of clinical trial of medicinal product in case of significant changes
Charter and questionnaire form of the client
Report for the implementation of the goals for 2010 and ratified goals for 2011.
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ADMINISTRATION & DEPARTMENTS
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Department «Legal, Administrative, Financial Activities and Quality Management»
Department «Marketing Authorisation of Medicinal Products»
Department «Market Supervision and Inspections»
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Department «Control of Blood Transfusion System»
Department «Medicinal product analyses»
Department «Medicinal Products Information and Noninterventional Researches»
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EMA reviews diabetes medicine canagliflozin
PRAC concludes review of medicines containing factor VIII
Pharmacovigilance / «Citizens»
Announcements
EMA reviews diabetes medicine canagliflozin
PRAC concludes that diabetes medicine canagliflozin may contribute to risk of toe amputation Risk may also apply to other medicines in the same class
PRAC reviewing safety of pulmonary hypertension medicine Uptravi
PRAC concludes assessment of gadolinium agents used in body scans and recommends regulatory actions, including suspension for some marketing authorisations Review finds evidence of gadolinium deposits in the brain after MRI body scans but no signs of harm
PRAC concludes review of medicines containing factor VIII
EMA reviews multiple sclerosis medicine Zinbryta
PRAC concludes there is no evidence of a change in the known risk of neutropenic enterocolitis cases with docetaxel
EMA restricts use of multiple sclerosis medicine Zinbryta
PRAC confirms restrictions on the use of linear gadolinium agents
EMA seeks views of public during its safety review of valproate
PRAC recommends that injectable methylprednisolone products containing lactose must not be given to patients allergic to cow's milk proteins
PRAC recommends modified-release paracetamol be removed from market
PRAC confirms its previous conclusion on risk of inhibitor development with factor VIII medicines
EMA starts new review of hydroxyethyl-starch containing medicines
EMA starts review of Esmya for uterine fibroids
Warning about use of prostate cancer medicine Xofigo in combination with Zytiga and prednisone or prednisolone
PRAC recommends suspending hydroxyethyl-starch solutions for infusion from the market
Women taking Esmya for uterine fibroids to have regular liver tests while EMA review is ongoing
PRAC recommends new measures to avoid valproate exposure in pregnancy New restrictions on use; pregnancy prevention programme to be put in place
PRAC recommends updating measures for pregnancy prevention during retinoid use Warning on possible risk of neuropsychiatric disorders also to be included for all oral retinoids
Prostate cancer medicine Xofigo must not be used with Zytiga and prednisone/prednisolone. Ongoing clinical study shows an increased risk of death and fractures with the combination
EMA reviewing risk of dosing errors with methotrexate - Review prompted by continued reports of overdose
PRAC recommends new measures to minimise risk of rare but serious liver injury with Esmya for fibroids
PRAC recommends restricting use of prostate cancer medicine Xofigo
PRAC recommends cautious use of Xeljanz for all patients at high risk of blood clots
PRAC recommends measures to minimise risk of serious side effects with Lemtrada for multiple sclerosis
PRAC confirms four-week limit for use of high-strength estradiol creams
Restrictions in use of cyproterone due to meningioma risk
Leuprorelin depot medicines: PRAC recommends new measures to avoid handling errors
PRAC recommends restricted use for bromocriptine in inhibiting post-partum lactation
PRAC recommends further measures to minimise risk of blood vessel blockage with Iclusig PRAC recommendations to be considered by CHMP for final opinion
PRAC review does not confirm increase in heart problems with testosterone medicines Committee recommends medicines can continue to be given for their authorised uses
PRAC recommends strengthening the restrictions on the use of valproate in women and girls Women to be better informed of the risks of valproate use during pregnancy
PRAC recommends measures to reduce risk of heart problems with Corlentor/Procoralan (ivabradine)
PRAC recommends updating advice on use of high-dose ibuprofen
Review of Tysabri started
Start of review of inhaled corticosteroids for chronic obstructive pulmonary disease
EMA to further clarify safety profile of human papillomavirus (HPV) vaccines
Start of review of nasal and mouth sprays containing fusafungine
SGLT2 inhibitors: PRAC makes recommendations to minimise risk of diabetic ketoacidosis
Updated recommendations to minimise the risk of the rare brain infection PML with Tysabri
EMA reviews direct-acting antivirals for hepatitis C
PRAC reviews known risk of pneumonia with inhaled corticosteroids for chronic obstructive pulmonary disease
Inhibitor development in previously untreated patients with severe haemophilia A treated with recombinant factor VIII products
PRAC warns of risk of hepatitis B re-activation with direct-acting antivirals for hepatitis C
EMA to review certain injectable medicines to treat allergy
PRAC concludes that diabetes medicine canagliflozin may contribute to risk of toe amputation Risk may also apply to other medicines in the same class
PRAC reviewing safety of pulmonary hypertension medicine Uptravi
EMA to review persistence of side effects known to occur with quinolone and fluoroquinolone antibiotics
New review of valproate use in pregnancy and women of childbearing age
PRAC concludes assessment of gadolinium agents used in body scans and recommends regulatory actions, including suspension for some marketing authorisations Review finds evidence of gadolinium deposits in the brain after MRI body scans but no signs of harm
PRAC investigates cancer medicine docetaxel
PRAC concludes review of medicines containing factor VIII
PRAC recommends new measures to avoid dosing errors with methotrexate
Administrative information
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To the attention of healthcare professionals, patients and citizens
European Medicines Agency starts review of ibuprofen medicines
PRAC recommends further measures to minimise risk of blood vessel blockage with Iclusig PRAC recommendations to be considered by CHMP for final opinion
PRAC review does not confirm increase in heart problems with testosterone medicines Committee recommends medicines can continue to be given for their authorised uses
PRAC recommends strengthening the restrictions on the use of valproate in women and girls Women to be better informed of the risks of valproate use during pregnancy
PRAC recommends measures to reduce risk of heart problems with Corlentor/Procoralan (ivabradine)
PRAC recommends new measures to minimise known heart risks of hydroxyzine-containing medicines Medicines can still be given for their approved uses, with new restrictions
PRAC recommends restrictions on the use of codeine for cough and cold in children
PRAC recommends updating advice on use of high-dose ibuprofen
Start of review of nasal and mouth sprays containing fusafungine
Review concludes evidence does not support that HPV vaccines cause CRPS or POTS
Updated recommendations to minimise the risk of the rare brain infection PML with Tysabri
SGLT2 inhibitors: PRAC makes recommendations to minimise risk of diabetic ketoacidosis
EMA recommends new safety measures for Zydelig
EMA reviews direct-acting antivirals for hepatitis C
EMA reviewing gadolinium contrast agents used in MRI scans
PRAC reviews known risk of pneumonia with inhaled corticosteroids for chronic obstructive pulmonary disease
EMA reviews diabetes medicine canagliflozin
EMA to review modified-release paracetamol
PRAC concludes review of Zydelig and issues updated recommendations for use EMA’s Pharmacovigilance Risk Assessment Committee (PRAC) has completed its review of Zydelig
Practice run on public hearings
Extension of the scope of a safety review
Review of factor VIII medicines begins
EMA starts review of retinoid medicines
New review of valproate use in pregnancy and women of childbearing age
PRAC investigates cancer medicine docetaxel
EMA reviews multiple sclerosis medicine Zinbryta
MEASURES FOR PREVENTION OF WNV TRANSFUSION TRANSMISSION – 2019
Pharmacovigilance
Announcements
Bulletins «Adverse drug reactions»
PRAC recommends restrictions on the use of codeine for cough and cold in children
Review of diabetes medicines called SGLT2 inhibitors started
EMA recommends new safety measures for Zydelig
EMA reviewing gadolinium contrast agents used in MRI scans
Use of metformin to treat diabetes now expanded to patients with moderately reduced kidney function
PRAC concludes that diabetes medicine canagliflozin may contribute to risk of toe amputation Risk may also apply to other medicines in the same class
PRAC reviewing safety of pulmonary hypertension medicine Uptravi
PRAC concludes assessment of gadolinium agents used in body scans and recommends regulatory actions, including suspension for some marketing authorisations Review finds evidence of gadolinium deposits in the brain after MRI body scans but no signs of harm
PRAC concludes there is no clear and consistent evidence of a difference in inhibitor development between classes of factor VIII medicines
PRAC confirms restrictions on the use of linear gadolinium agents
EMA seeks views of public during its safety review of valproate
PRAC recommends that injectable methylprednisolone products containing lactose must not be given to patients allergic to cow's milk proteins
PRAC recommends modified-release paracetamol be removed from market
PRAC confirms its previous conclusion on risk of inhibitor development with factor VIII medicines
EMA starts new review of hydroxyethyl-starch containing medicines
Warning about use of prostate cancer medicine Xofigo in combination with Zytiga and prednisone or prednisolone
PRAC recommends suspending hydroxyethyl-starch solutions for infusion from the market
Women taking Esmya for uterine fibroids to have regular liver tests while EMA review is ongoing
PRAC recommends new measures to avoid valproate exposure in pregnancy New restrictions on use; pregnancy prevention programme to be put in place
PRAC recommends updating measures for pregnancy prevention during retinoid use Warning on possible risk of neuropsychiatric disorders also to be included for all oral retinoids
Prostate cancer medicine Xofigo must not be used with Zytiga and prednisone/prednisolone. Ongoing clinical study shows an increased risk of death and fractures with the combination
EMA reviewing risk of dosing errors with methotrexate - Review prompted by continued reports of overdose
PRAC recommends new measures to minimise risk of rare but serious liver injury with Esmya for fibroids
Fluoroquinolone and quinolone antibiotics: PRAC recommends restrictions on use
PRAC recommends new measures to avoid dosing errors with methotrexate
PRAC recommends cautious use of Xeljanz for all patients at high risk of blood clots
PRAC recommends measures to minimise risk of serious side effects with Lemtrada for multiple sclerosis
Restrictions in use of cyproterone due to meningioma risk
New testing and treatment recommendations for fluorouracil, capecitabine, tegafur and flucytosine
Suspension of ulipristal acetate for uterine fibroids during ongoing EMA review of liver injury risk
NCA for blood
NCA for blood
MEASURES FOR PREVENTION OF WNV TRANSFUSION TRANSMISSION – 2021
MEASURES FOR PREVENTION OF WNV TRANSFUSION TRANSMISSION – 2022
MEASURES FOR PREVENTION OF WNV TRANSFUSION TRANSMISSION – 2024
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Important!
From 01.01.2010 the submission of the documentation in electronic format - eCTD or NeeS is obligatory.
Important!
To the attention of holders of marketing authorizations
Dear applicants,
To the attention of all Marketing Authorisation Holders
COVID-19
Companies menu
Information for companies
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TO ALL APPLICANTS, MARKETING AUTHORIZATION HOLDERS AND THEIR LOCAL REPRESENTATIVES
TO THE APPLICANTS, MARKETING AUTHORIZATION HOLDERS AND THEIR REPRESENTATIVES
Marketing authorisation of medicinal products
Fees
Bulgaria as a Reference Member State (RMS) for decentralized (DCP)/ mutual recognition (MRP) procedures for marketing authorization of medicinal products
Medical devices
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Guidelines
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Instructions to the submitters for preparation of a list of medical devices
Forms
Medicinal information
Linguistic check
Pharmacovigilance / «Companies»
Single, central platform now mandatory for all periodic safety update reports
Clinical trials
Draft proposal for an addendum, on transparency, to the “Functional specifications for the EU portal and EU database to be audited"
NOTICE TO SPONSORS OF CLINICAL TRIALS
Ethics Committee
Ethics Committee for Multicenter Trials
Control of the medicinal products
List of GMP inspectors and experts
Announcements - Medical devices
Гръдните импланти на френската фирма PIP (“Poly Implant Prothese”) – изтеглени от пазара
Доклад на EBA Europheresis Group
Блокиране на медицински изделия - дезинфекциращи кърпички на производителя “TRIAD GROUP”, САЩ
Гръдни импланти на френската фирма PIP (“Poly Implant Prothese”) – резултати от тестове
Pharmacopoeia
Announcements for pharmacovigilance
To the attention of all Marketing Authorisation Holders
EU regulations / «Pharmacovigilance»
"The rules governing medicinal products in the European Union" / Volume 9
BDA instructions / «Pharmacovigilance»
E-reporting / «Pharmacovigilance»
Expedited reporting requirements of the Bulgarian Drug Agency(BDA) for Individual Case Safety reports
Reporting rules for MAHs/sponsors of CTs after 22nd November 2017
CESP
National requirements:
Important!
COVID-19
Administrative information
Over-the-Counter Drugs (OTC)
List of medicinal products under additional monitoring
EMA: Medicines under additional monitoring
Публични оценъчни доклади
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