ONSTYLE

Standardized and compliant documents in seconds

Having everyone at a biopharma company precisely following the latest, strict document-standards is nearly unachievable. Also, checking compliance with both company standards and industry regulations takes a lot of time. Clearly, an automated solution is needed that manages all Word documents and makes them standardized as well as compliant with a single click.

HOW DACHS CAN HELP

Introducing OnStyle

Our Word add-in helps eliminate frustration from violating the company and external requirements for all employees. OnStyle can change how documents are created in the submission process with regulatory specific, built-in checks, making the whole process fast and easy.
Alignment with industry document formatting standards (e.g.:FDA, EMA) is already built in, while additional company-related document formatting standards can be easily integrated.

With OnStyle, the overall review of documents is achieved with a single click that helps avoiding all forms of accidental mistakes.

Save time and effort
OnStyle helps automating all forms of compliance with company and external regulations, therefore submission deadlines can be met easily. Instead of editing documents for hours, the focus is back on content creation, making processes significantly more efficient.

Don’t fear the PDF
The dreaded discrepancy between the original Word and converted PDF documents is a thing of the past: enjoy perfectly consistent PDF generation for OnStyle adjusted documents.

OnStyle features

  • Customization of your company document formatting standards: layouts can be defined for paragraphs, headings, tables, abbreviations, capitalization, hyphens/dashes, bullets and lists, spelling, typos, numbers, table/figure numbering, etc.
  • Centrally controlled, standard management for differentiated user groups
  • Document conversion tool: easily apply company standards to any document
  • Checking options with one-click trackable automatic corrections: comparing document layout to company standards and showing alterations
  • Controlled, automated direct content change, conversions to standards are only made once automated offers are accepted
  • Creating healthy documents, eliminating known errors: preparing documents for easy and fast conversion to high-quality PDF (smaller files, faster conversion)
  • Multiple language support (dedicated tool with special configuration principles)

WHY TRUST DACHS

Standardized and compliant documents in seconds

Having everyone at a biopharma company precisely following the latest, strict document-standards is nearly unachievable. Also, checking compliance with both company standards and industry regulations takes a lot of time. Clearly, an automated solution is needed that manages all Word documents and makes them standardized as well as compliant with a single click.

HOW DACHS CAN HELP

Introducing OnStyle

Our Word add-in helps eliminate frustration from violating the company and external requirements for all employees. OnStyle can change how documents are created in the submission process with regulatory specific, built-in checks, making the whole process fast and easy.
Alignment with industry document formatting standards (e.g.:FDA, EMA) is already built in, while additional company-related document formatting standards can be easily integrated.

With OnStyle, the overall review of documents is achieved with a single click that helps avoiding all forms of accidental mistakes.

Save time and effort
OnStyle helps automating all forms of compliance with company and external regulations, therefore submission deadlines can be met easily. Instead of editing documents for hours, the focus is back on content creation, making processes significantly more efficient.

Don’t fear the PDF
The dreaded discrepancy between the original Word and converted PDF documents is a thing of the past: enjoy perfectly consistent PDF generation for OnStyle adjusted documents.

OnStyle features

  • Customization of your company document formatting standards: layouts can be defined for paragraphs, headings, tables, abbreviations, capitalization, hyphens/dashes, bullets and lists, spelling, typos, numbers, table/figure numbering, etc.
  • Centrally controlled, standard management for differentiated user groups
  • Document conversion tool: easily apply company standards to any document
  • Checking options with one-click trackable automatic corrections: comparing document layout to company standards and showing alterations
  • Controlled, automated direct content change, conversions to standards are only made once automated offers are accepted
  • Creating healthy documents, eliminating known errors: preparing documents for easy and fast conversion to high-quality PDF (smaller files, faster conversion)
  • Multiple language support (dedicated tool with special configuration principles)

WHY TRUST DACHS

20+ YEARS OF EXPERIENCE

DACHS has supported 100 000 + submissions in the last 10 years. We look back on over 20 years of experience in the field of document management for Life Sciences by providing software development and support in fields of drug development, clinical trial documentation and tracking, regulatory submissions, as well as drug manufacturing, packaging and labelling.

20+ YEARS OF EXPERIENCE

DACHS has supported 100 000 + submissions in the last 10 years. We look back on over 20 years of experience in the field of document management for Life Sciences by providing software development and support in fields of drug development, clinical trial documentation and tracking, regulatory submissions, as well as drug manufacturing, packaging and labelling.

DACHS, THE SUBMISSION EXPERT

DACHS’ professionals are able to reliably provide as well as flexibly adapt their services to changing requirements in a regulatory environment. As trusted partners of Industry Leading Pharma Clients, we are fully committed to our clients’ best possible business outcomes.

DACHS, THE SUBMISSION EXPERT

DACHS’ professionals are able to reliably provide as well as flexibly adapt their services to changing requirements in a regulatory environment. As trusted partners of Industry Leading Pharma Clients, we are fully committed to our clients’ best possible business outcomes.

ISTVÁN AGG
Director of Business Development
 
+41 61 508 0300

ISTVÁN AGG
Head of Solution Delivery

+41 61 508 0300

Contact us for further details

Contact us for further details