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HORN Pharmaceutical Consulting provides regulatory and business advice to companies from the pharmaceutical, biotechnology and medical device industries. We offer a full spectrum of global consulting services and solutions from early phases of product development and clinical trials to submission of marketing authorization applications.
Whether you are a pharmaceutical or biotechnology company, an API (Active Pharmaceutical Ingredient) manufacturer, contract manufacturer, contract laboratory, SME (Small and Medium-sized Enterprise), medical device industry, Advanced Therapy Industry (ATI), we will help you carry out both large and small projects in all stages of the product lifecycle: in the pre-submission, submission, pre-approval, approval and post-approval phase.
Our internationally ...experienced specialists have detailed know-how in the planning and preparation of dossiers, e.g. European ASMF (Active Substance Master File), US-DMF (Drug Master File), certificate of suitability (CEP). We prepare regulatory documents for your global submission. For the start of the clinical trial the CTA (Clinical Trial Application) needs to be submitted in EU, and the IND (Investigational New Drug Application) needs to be submitted in US. These are the documents which we will be elaborated with you and will be written for you.
Once you have successfully gone through clinical trials we support you in the preparation of the CTD (Common Technical Document) for submission of the European MAA (Marketing Authorization Application) and the US NDA (New Drug Application) / BLA (Biologic License Application).
Regulatory submissions entail a large variety of documents. We are here to advice you on how to structure and write these documents, and we are prepared to take up this task for you, e.g. SPCs (Summary of Product Characteristics), clinical or nonclinical study protocols and reports, clinical or non-clinical summaries and overviews, Quality Overall Summaries (QOS) as well as CMC documents.
We guide your project through the regulatory process, elaborate regulatory strategies for European and US-filings, and help you in the preparation of meetings with Authorities (national agencies, EMEA, FDA).
However, a successful submission also depends on compliance with GMP / GCP and GLP standards. We check your compliance status during mock inspections. We help you to ensure adherence to EU and US-requirements and support you in setting up adequate quality systems by writing SOPs and performing training for your personnel.
We are committed to supporting you make substantial performance improvement. With every customer we build dynamic multidisciplinary teams to thoroughly match individual applications to the constantly evolving regulatory demands.
Trust us because quality matters! Read more
Whether you are a pharmaceutical or biotechnology company, an API (Active Pharmaceutical Ingredient) manufacturer, contract manufacturer, contract laboratory, SME (Small and Medium-sized Enterprise), medical device industry, Advanced Therapy Industry (ATI), we will help you carry out both large and small projects in all stages of the product lifecycle: in the pre-submission, submission, pre-approval, approval and post-approval phase.
Our internationally ...experienced specialists have detailed know-how in the planning and preparation of dossiers, e.g. European ASMF (Active Substance Master File), US-DMF (Drug Master File), certificate of suitability (CEP). We prepare regulatory documents for your global submission. For the start of the clinical trial the CTA (Clinical Trial Application) needs to be submitted in EU, and the IND (Investigational New Drug Application) needs to be submitted in US. These are the documents which we will be elaborated with you and will be written for you.
Once you have successfully gone through clinical trials we support you in the preparation of the CTD (Common Technical Document) for submission of the European MAA (Marketing Authorization Application) and the US NDA (New Drug Application) / BLA (Biologic License Application).
Regulatory submissions entail a large variety of documents. We are here to advice you on how to structure and write these documents, and we are prepared to take up this task for you, e.g. SPCs (Summary of Product Characteristics), clinical or nonclinical study protocols and reports, clinical or non-clinical summaries and overviews, Quality Overall Summaries (QOS) as well as CMC documents.
We guide your project through the regulatory process, elaborate regulatory strategies for European and US-filings, and help you in the preparation of meetings with Authorities (national agencies, EMEA, FDA).
However, a successful submission also depends on compliance with GMP / GCP and GLP standards. We check your compliance status during mock inspections. We help you to ensure adherence to EU and US-requirements and support you in setting up adequate quality systems by writing SOPs and performing training for your personnel.
We are committed to supporting you make substantial performance improvement. With every customer we build dynamic multidisciplinary teams to thoroughly match individual applications to the constantly evolving regulatory demands.
Trust us because quality matters! Read more
Other Products
- GMP Consulting
- GMP Education & Training