Design Controls: Introductory

Design Controls: Introductory

Design Controls — 21 CFR §820.30 Vocabulary and Sub-Clause Orientation

Design Controls: Introductory

Build a working foundation in 21 CFR §820.30 Design Controls — the vocabulary, sub-clauses, and the alignment with ISO 13485:2016 §7.3 that anchor medical-device design and development.

RAQ-610-IIntroductory16 hoursCertificate of Completion

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Design Controls
FormatProfessional Certificate Course
LevelIntroductory
Duration16 hours
LanguageEnglish
CertificateCertificate of Completion — Aleph University
Full course trackIntroductory (16 h) + Advanced (32 h) = 48 hours
Prerequisite / Recommended Preparation

No prior Aleph course is required.

Overview

Design Controls are the disciplined framework by which medical-device manufacturers translate a defined clinical need into a verified, validated, transferable product. The FDA codifies the framework in 21 CFR §820.30 — soon governed by the QMSR (effective February 2, 2026, with ISO 13485:2016 incorporated by reference). The framework is structured around ten sub-clauses (a)–(j) covering scope, planning, inputs, outputs, review, verification, validation, transfer, changes, and the Design History File. Design Controls failures appear repeatedly in FDA Warning Letters and in the root-cause analysis of recalled devices.

This 16-hour Professional Certificate Course is the entry point of the Aleph Design Controls course track. It introduces the 21 CFR §820.30 framework; the ten sub-clauses at orientation depth; the canonical distinction between Design Verification (§820.30(f), “did we build the product right?”) and Design Validation (§820.30(g), “did we build the right product?”); the role of Design Review (§820.30(e)) as cross-functional governance; the Design History File (§820.30(j)) as the auditable record of the design effort; and the alignment with ISO 13485:2016 §7.3 Design and Development.

The course prepares participants for the Advanced level (`RAQ-610-A`), where the same content is exercised at applied depth — applied Design Input authoring, applied Design Output mapping, applied Design Review governance, applied V&V planning, applied Design Transfer planning, applied Design Change handling, and an authored Design History File for a chosen device. Together the Introductory and Advanced levels form a 48-hour course track.

What you will learn
Explain the 21 CFR §820.30 framework and its alignment with ISO 13485:2016 §7.3.
Identify the ten sub-clauses of §820.30 (a)–(j) and the role of each.
Distinguish Design Input (§820.30(c)) from Design Output (§820.30(d)) and recognize bidirectional traceability.
Distinguish Design Verification (§820.30(f)) from Design Validation (§820.30(g)).
Recognize the role of Design Review (§820.30(e)) at each stage gate.
Recognize the role of Design Transfer (§820.30(h)) and Design Changes (§820.30(i)).
Recognize the structure and content expectations of the Design History File (§820.30(j)).
Articulate where the rest of the course track (Advanced level) extends each topic into applied work.
course topics & modules
Professional relevance

The Introductory course establishes the Design Controls vocabulary the medical-device industry expects of any professional with a stake in design-program compliance. Employers in this space include medical-device manufacturers, IVD manufacturers, and consultancies serving manufacturers.

Certificate of Completion

Participants who meet the course completion requirements receive a Certificate of Completion issued by Aleph University.

Completion of both the Introductory and Advanced levels may be reviewed by Aleph University for potential recognition within an applicable graduate pathway, subject to institutional review and applicable academic policies. Recognition is not automatic and is not guaranteed.
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