About Us

Your regulatory partner for entering the Saudi market with confidence

Business Dream (formerly Dream Works) is a Saudi regulatory consultancy specialized in medical device and medical product registration with the Saudi Food and Drug Authority (SFDA), and in authorized representation for foreign manufacturers. We combine in-depth regulatory knowledge with hands-on field experience.

Our Story

Field experience turned into a proven methodology

Business Dream was founded on a simple belief: manufacturers and importers deserve a partner who truly understands regulatory requirements and saves them time, cost, and rounds of deficiency letters. Through years of daily work on registration files, we built a clear methodology that starts with understanding the product and classifying it correctly, and ends with obtaining approval and supporting post-market obligations.

What we do

  • Medical device and medical product registration with the SFDA
  • Authorized representation for foreign manufacturers in Saudi Arabia
  • Product classification and regulatory pathway determination
  • Technical file preparation and pre-submission review
  • Application follow-up and handling of SFDA queries
  • SABER and conformity certificates

Who we serve

  • Foreign manufacturers seeking access to the Saudi market
  • Local agents, distributors, and importers
  • Emerging national manufacturers in the medical sector
  • Healthcare and commercial entities needing regulatory advice
Founder

Fahad Mohammed Abdullah Almasaari

Founder & Owner — Business Dream

12+ years in regulatory affairs

Fahad Almasaari brings more than twelve years of experience in medical device and medical product regulatory affairs in Saudi Arabia. Over these years, he has guided manufacturers and importers through every stage of the regulatory journey — from product classification and technical file preparation, through submission and query resolution, to marketing authorization and post-market obligations.

He founded Business Dream to offer clients what he himself looked for early in his career: clear requirements, honest assessments, and on-time delivery.

Areas of expertise

  • Medical Device Marketing Authorization (MDMA) applications
  • SFDA classification rules for medical and IVD devices
  • EU MDR and IVDR requirements
  • Technical file preparation and review
  • Authorized Representative role and obligations
  • Medical storage and Good Distribution Practice
What Guides Us

Our vision, mission, and values

01

Vision

To be the most trusted regulatory partner for manufacturers and importers entering the Saudi medical device and medical product market.

02

Mission

To simplify our clients' regulatory journey through precise advice, complete submission files, and continuous follow-up — bringing their products to patients and users faster and safely.

03

Values

Attention to detail, transparent assessments, commitment to deadlines, and strict confidentiality of client data.

Why Business Dream?

What sets us apart

Hands-on experience

More than 12 years of daily work on registration files and SFDA deficiency responses.

Honest pre-assessment

We review your documents before submission and clearly identify gaps, reducing query rounds and delays.

Clear communication

A single point of contact who follows your file and keeps you informed at every stage.

Local market knowledge

Based in Riyadh, we know the Saudi market's requirements and procedural details.

End-to-end service

From classification and registration to authorized representation and conformity certificates — all in one place.

Confidentiality & commitment

We handle manufacturers' data and technical documentation with full confidentiality and professional responsibility.

Let's bring your products to the Saudi market

Riyadh, Saudi Arabia · 00966540000260 · info@works.com.sa

Contact Us
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