不良事件报告

如果发生不良事件,患者应始终寻求医生或药剂师的建议。

如果您想向ELC Group s.r.o.报告不良事件,请在下面找到联系信息:

+420 224 910 672

(欧洲中部时间09.00-17.30)

+420 226 251 459

(24/7不间断)

有关其他任何问题,请与我们联系:

+420 22 491 0000或我们的 区域办事处。

Hlášení nežádoucích príhod

Pacienti by meli vždy požádat o radu svého lékare nebo lékárníka v prípade výskytu nežádoucích príhod.

Pokud chcete nahlásit nežádoucí príhodu spolecnosti ELC Group s r.o., prosím využijte kontaktních údaju níže:

+420 224 910 672

(09.00-17.30 CET)

+420 226 251 459

(non-stop 24/7)

Pro záležitosti, které se netýkaji farmakovigilance, kontaktujte prosím recepci:

+420 22 491 0000 nebo naše další pobočky.

How recent moves by the FDA spell good news for generics in the US

On October 2nd 2017, the FDA held a 2-day meeting to discuss how generic drug development – especially that for complex generics – could be better streamlined. The FDA has clearly noticed that competition in the complex generic space is increasingly slow and hard to generate and, as such, it has released two new draft guidance documents.

The first draft guidance document relates to formal meetings between FDA and ANDA applicants, and ANDAs for certain highly purified synthetic peptide drug products that refer to listed drugs of rDNA origin. This guidance will help to assist potential as well as actual applicants in generating meeting requests and with their subsequent submissions. The guidance also helps to navigate the meeting package required for complex products, as per GDFUA II (Generic Drug User Fee Amendments Reauthorization of 2017).

The second draft guidance document is aimed at helping perspective ANDA applicants determine whether a submission for certain synthetic peptide drugs should be submitted as an ANDA as opposed to an NDA. This centres primarily on the complex issue of establishing bioequivalence for these products due to difficulties in blood level detection, or a product’s localised as opposed to systemic mechanism of action.

The above documents follow a growing trend from the FDA. In fact, back in June, the FDA took two major steps to opening up generic competition. The first was a release of a list containing off-patent products with little or no competition. The list is split into two parts: part I of the list identifies those drug products for which the FDA could immediately accept an ANDA without prior discussion, while part II identifies drug products involving potential legal, regulatory, or scientific issues which should be addressed with the Agency prior to submission of an ANDA. The second step was prioritising the review of abbreviated new drug applications (ANDAs) for which there are fewer than three ANDAs approved for the reference listed drug. The aim of this step is to free up competition and to tackle the growing cost of healthcare.

The regulatory landscape for generics across the globe is constantly evolving and at ELC Group we can help identify and harness new areas of business growth and portfolio expansion through these emerging regulatory channels and opportunities.

相关新闻